Microtensiometer technique for in situ measurement of soil matric potential and root water extraction from a sandy soil

The suitability of microtensiometers to measure the spatial variation of soil matric potential and its diurnal change was tested in a pot experiment with pearl millet (Pennisetum americanum [L.] Leeke) in a sandy soil as the soil dried out.The temporal and spatial resolution of this technique allowed precise measurement of soil matric potential and thus estimation of soil water extraction from different compartments as well as from the whole rooting zone. The technique also allowed the measurement of rehydration of plants at night and root water uptake rate per unit soil volume or per unit root length. The precision of determination of root water uptake depended greatly on the accuracy of the estimate of hydraulic conductivity, which was derived from a bare soil and might be different for a cropped soil owing to aggregation induced by the root system. A linear relationship between root length and water uptake was found (r²=0.82), irrespective of variation in soil water content between compartments and despite the variation in root age, xylem differentiation and suberin formation expected to exist between different compartments of the rooting zone. As the experiment was carried out in a range of soil matric potentials between –4 and –30 kPa, drought stress did not occur. Further information at lower soil matric potentials are required, to address questions such as the importance of soil resistance for water uptake, or which portion of the root system has to be stressed to induce hormonal signals to the shoot. The microtensiometer technique can be applied to soil matric potentials up to –80 kPa.     

The gradient between pre-dawn rhizoplane and bulk soil matric potentials, and its relation to the pre-dawn root and leaf water potentials of four species

Uptake of soil water by plants may result in significant gradients between bulk soil and soil in the vicinity of roots. Few experimental studies of water potential gradients in close proximity to roots, and no studies on the relationship of water potential gradients to the root and leaf water potentials, have been conducted. The occurrence and importance of pre-dawn gradients in the soil and their relation to the pre-dawn root and leaf water potentials were investigated with seedlings of four species. Pre-germinated seeds were grown without watering for 7 and lid in a silt loam soil with initial soil matric potentials of -0.02, -0.1 and -0.22 MPa. Significant gradients, independent of the species, were observed only at pre-dawn soil matric potentials lower than -0.25 MPa; the initial soil matric potentials were -0.1 MPa. At an initial bulk soil matric potential of -0.22 MPa, a steep gradient between bulk and rhizoplane soil was observed after 7 d for maize (Zea mays L. cv. Issa) and sunflower (Helianthus annuus L. cv. Nanus), in contrast to barley (Hordeum vulgare L. cv. Athos) and wheat (Triticum aestivum L. cv. Kolibri). Pre-dawn root water potentials were usually about the same as the bulk soil matric potential and were higher than the rhizoplane soil matric potential. Pre-dawn root and leaf water potentials tended to be much higher than rhizoplane soil matric potentials when the latter were lower than -0.5 MPa. It is concluded that plants tend to become equilibrated overnight with the wetter bulk soil or with wetter zones in the bulk soil. Plants can thus circumvent negative effects of localized steep pre-dawn soil matric potential gradients. This may be of considerable importance for water uptake and growth in drying soil.     

Root:soil adhesion in the maize rhizosphere: the rheological approach

This study was designed to investigate the strength of attachment of plant seedling roots to the soil in which they were grown. The study also assessed the effects of differing soil textures and differing soil matric potentials upon the strength of the root:soil attachment. A device for growing roots upon a soil surface was designed, and was used to produce roots which were attached to the soil. In order to quantify root:soil adhesion, roots of maize seedlings, grown on the soil surface, were subsequently peeled off using a universal test machine, in conjunction with simultaneous time-lapse video observation. To clarify the partitioning of energy in the root:soil peeling test, separate mechanical tests on roots, and on two adherent remoulded topsoil balls were also carried out. The seedling root was characterised by a low bending stiffness. The energy stored in bending was negligible, compared to the root:soil adhesion energy. The mechanical properties of two adherent remoulded topsoil balls were a decrease of the soil:soil adhesion energy as the soil:soil plastic energy increased. These two parameters were therefore interdependent. Using a video-camera system, it was possible to separate the different processes occurring during the root:soil peeling test, in particular, the seed:soil adhesion and the root:soil soil adhesion. An interpretation of the complex and variable force:displacement curves was thus possible, enabling calculation of the root:soil interfacial rupture energy. At a given suction (10 kPa), the results of the peeling test showed a clear soil texture effect on the value of the root:soil interfacial rupture energy. In contrast, for the same silty topsoil, the effect of the soil water suction on the value of the interfacial rupture energy was very moderate. The root:soil interfacial rupture energy was controlled mainly by a product of microscopic soil specific surface area and the macroscopic contact surface area between the root and the soil. Biological and physical interactions contributing to root:soil adhesion such as root:soil interlocking mechanics were also analysed and discussed. This revised version was published online in June 2006 with corrections to the Cover Date.     

Influence of root density on the critical soil water potential

Estimation of root water uptake in crops is important for making many other agricultural predictions. This estimation often involves two assumptions: (1) that a critical soil water potential exists which is constant for a given combination of soil and crop and which does not depend on root length density, and (2) that the local root water uptake at given soil water potential is proportional to root length density. Recent results of both mathematical modeling and computer tomography show that these assumptions may not be valid when the soil water potential is averaged over a volume of soil containing roots. We tested these assumptions for plants with distinctly different root systems. Root water uptake rates and the critical soil water potential values were determined in several adjacent soil layers for horse bean (Vicia faba) and oat (Avena sativa) grown in lysimeters, and for field-grown cotton (Gossypium L.), maize (Zea mays) and alfalfa (Medicago sativa L.) crops. Root water uptake was calculated from the water balance of each layer in lysimeters. Water uptake rate was proportional to root length density at high soil water potentials, for both horse bean and oat plants, but root water uptake did not depend on root density for horse bean at potentials lower than −25 kPa. We observed a linear dependency of a critical soil water potential on the logarithm of root length density for all plants studied. Soil texture modified the critical water potential values, but not the linearity of the relationship. B E Clothier Section editor     

膜下滴灌土壤湿润范围对棉花根层土壤水热环境和根系耗水的影响

为探明膜下滴灌土壤湿润范围对棉花根区水热环境及棉花根系耗水的影响,设置滴头流量1.69（W₁₆₉）、3.46（W₃₄₆）和6.33 L·h^-1（W₆₃₃）3个水平,观测分析了棉花生育期土壤基质势、土壤温度及棉花根系生长和耗水分布状况.结果表明： 膜下滴灌土壤温度主要受光照影响;不同类型土壤湿润区之间的土壤温度差异不明显,不同土壤湿润区的膜下土壤温度对棉花根系耗水也没有明显影响.但是随着土壤湿润区由窄深型向宽浅型过渡,棉花根区土壤基质吸力在水平方向上分布更趋于均匀,而棉花根系耗水强度主要受土壤基质吸力分布的影响.宽浅型土壤湿润区（W₆₃₃）的棉花膜下内、边行根系耗水强度差值平均为0.67 mm·d^-1,有利于内、边行棉株生长整齐;窄深型土壤湿润区（W₁₆₉）的内、边行根系耗水强度差值平均为0.88 mm·d^-1,不利于内、边行棉株均匀生长.可见,膜下滴灌技术设计中,土壤湿润区不应小于覆膜宽度,应使膜下土壤整体湿润.     

Long‐distance abscisic acid signalling under different vertical soil moisture gradients depends on bulk root water potential and average soil water content in the root zone

To determine how root‐to‐shoot abscisic acid (ABA) signalling is regulated by vertical soil moisture gradients, root ABA concentration ([ABA]_root), the fraction of root water uptake from, and root water potential of different parts of the root zone, along with bulk root water potential, were measured to test various predictive models of root xylem ABA concentration [RX‐ABA]_sap. Beans (Phaseolus vulgaris L. cv. Nassau) were grown in soil columns and received different irrigation treatments (top and basal watering, and withholding water for varying lengths of time) to induce different vertical soil moisture gradients. Root water uptake was measured at four positions within the column by continuously recording volumetric soil water content (θ_v). Average θ_v was inversely related to bulk root water potential (Ψ_root). In turn, Ψ_root was correlated with both average [ABA]_root and [RX‐ABA]_sap. Despite large gradients in θ_v, [ABA]_root and root water potential was homogenous within the root zone. Consequently, unlike some split‐root studies, root water uptake fraction from layers with different soil moisture did not influence xylem sap (ABA). This suggests two different patterns of ABA signalling, depending on how soil moisture heterogeneity is distributed within the root zone, which might have implications for implementing water‐saving irrigation techniques.     

Effect of soil strength on root growth under different water conditions

The objective of this study was to determine the effects of soil water and soil strength on root growth in situations where the individual effects of both of these factors were important. Three grain legumes were grown from pre-germinated seeds for five days on 50-mm compacted columns of two major soils of Sri Lanka. Four or five levels of bulk density (1.1 to 1.8 Mg.m^–3) and five or six levels of matric potential (–0.02 to–2.0 MPa) were used.Soil strength and matric potential effects on root growth were independently significant for most crop and soil combinations. Under high (wet) matric potential (>–0.77 MPa) soil conditions, the effect of soil water on root growth was evident only in its effect on soil strength. Bulk density had a significant effect on root growth independent of soil strength and matric potential in three cases.For all crops and soils, root penetration was 80% of the maximum or greater when the average soil strength (soil water not limiting) was 0.75 MPa or less, and when the average matric potential (soil strength not limiting) was –0.77 MPa or greater (wetter). Root penetration was 20% of the maximum or less when the soil strength was greater than 3.30 MPa (soil water not limiting), and when matric potential (soil strength not limiting) was less than –3.57 MPa. The use of pre-germinated seeds, which contained imbibed water, combined with a lack of water loss from the closed chambers containing the plants is the probable cause for the very low (–3.57 MPa) matric potential that allowed root growth at 20% of the maximum.     

Modeling soil water movement with water uptake by roots

Soil water movement with root water uptake is a key process for plant growth and transport of water and chemicals in the soil-plant system. In this study, a root water extraction model was developed to incorporate the effect of soil water deficit and plant root distributions on plant transpiration of annual crops. For several annual crops, normalized root density distribution functions were established to characterize the relative distributions of root density at different growth stages. The ratio of actual to potential cumulative transpiration was used to determine plant leaf area index under water stress from measurements of plant leaf area index at optimal soil water condition. The root water uptake model was implemented in a numerical model. The numerical model was applied to simulate soil water movement with root water uptake and simulation results were compared with field experimental data. The simulated soil matric potential, soil water content and cumulative evapotranspiration had reasonable agreement with the measured data. Potentially the numerical model implemented with the root water extraction model is a useful tool to study various problems related to flow transport with plant water uptake in variably saturated soils. This revised version was published online in June 2006 with corrections to the Cover Date.     

Water use and sodium chloride uptake by apple trees

Summary Apple trees grown with their root systems split into halves were used to study the effects of non-uniform salinity stress within a root system upon salt and water uptake. Water uptake declined rapidly when sodium chloride solution (90 meq l⁻¹) was added to any root zone but uptake increased correspondingly in the non-saline root zone of each tree. This changed pattern of water uptake with partial salinization did not change the total water use by the trees compared with their water use when neither root zone was salt stressed. After a‘steady-state’ condition of water uptake had been reached 80 to 85% of the water was taken up in the non-saline root zone. Irrigation at three soil matric potential intervals of −6.6, −33 and −66 kPa allowed to develop in the non-saline root zone of each tree did not affect water use responses. Leaf concentrations of Ca, Mg and K were unaffected by treatments. Chloride and Na concentrations increased in leaves with exposure to salinity stress in half root zones and with increasing soil matric potential stress. Some evidence was obtained using tritium enriched water that water was transferred from a non-saline root zone into a saline root zone but the volume involved was unmeasurable.     

Does Soil Strength Play a Role in Wheat Yield Losses Caused by Soil Drying?

Shoot growth in wheat is sensitive to high soil strength, but as high strength and drying tend to occur together it has proved difficult to separate the effects of water stress and mechanical impedance. The results of two field experiments in 2003 and 2004, where soil strength was manipulated by compaction and irrigation, demonstrated that the yield of wheat (Triticum aestivum L.) was sensitive to physical stress in the root zone. We obtained linear relationships between yield and soil strength and between yield and accumulated soil moisture data (accumulation analogous to thermal time), with similar slopes for both seasons. We were unable to detect root-sourced signals of xylem-sap ABA concentration, despite changes in stomatal conductance. When mechanical impedance and matric potential were varied independently in controlled environments, the growth of wheat was sensitive to mechanical impedance, but not to small changes in matric potential. While the response of stomatal conductance to soil drying in the field could be interpreted as evidence of hydraulic signalling, we suggest that the role of high soil strength, in limiting growth rates on moderately dry soil, requires further research.     

Occurrence of Inverted Water Potential Gradients between Soil and Bean Roots

Measurements with a pressure chamber were made of the xylem water potential of leaves, shoots and roots from bean plants (Pkaseolus vulgaris L. cv. Processor) grown with a 12 hour dark period and natural or artificial light conditions during the day. The water potentials were measured at the end of a dark period and during the light period. Measurements taken at the end of the dark period indicated normal potential gradients within the soil/plant system (leaf < shoot < root < soil), when the matric potential of soil water was relatively high (above ?0.02 bar), and the gradients then also remained normal during the day (natural light). When the soil water potential was ?1 bar or lower in the morning, however, the root xylem water potential was higher than the soil water potential; at very low soil water potentials (< ?4 bar) it remained higher during most of the day. In this case also leaf and shoot xylem water potentials were higher than the soil water potential in the early morning, although decreasing rapidly in daylight. Under artificial light, both leaf and root water potentials were higher than the soil water potential throughout the whole diurnal cycle when the latter potential was below ?4 bar. From measurements of stomatal diffusion resistance, transpiration, relative water content of leaves and of changes in the matric potential of soil water, it was concluded that when the matric potential of soil water was low, water could be taken up by the plant against a water potential gradient. Because leaf xylem water potential was always lower than root xylem water potential, the mechanism involved in the inversion of water potential gradient must be localized in the roots, and probably related to ion uptake. Symbols and abbreviations used in the text: Ψ: Plant water potential (thermocouple psychrometer); Ψx: Xylem water potential (pressure chamber); Ψs: Osmotic potential of xylem sap; Ψm: Matric potential of soil water; RWC: Relative water content.     

不同龄阶梭梭根区土壤水分时空变化特征

土壤水是荒漠植被发育最主要的制约因子。不仅影响植物的生长和发育,还限制着植被的种类、数量和分布。梭梭作为北方荒漠区重要的固沙植物,研究梭梭林地土壤水分动态对其植被生存或恢复以及群落稳定性维持具有重要意义。鉴于少有学者研究过不同龄阶梭梭根区的土壤含水率差异,于2014年2月至2014年11月,采用中子仪法和烘干法对0—400 cm沙层土壤含水率进行了原位观测,分析了不同龄阶梭梭根区土壤水分的时空变化规律。结果表明:(1)梭梭根区土壤水分时间变化可分为4个阶段:2月下旬—3月下旬是土壤水分快速补给期,4月上旬—5月下旬是土壤水分均衡期,6月上旬—10月下旬是土壤水分耗损期,11月上旬—次年2月中旬是土壤水分稳定期;(2)梭梭根区0—50 cm土层,受降雨、融雪水入渗补给和蒸发的影响较大,土壤水分变异系数较大且随深度增加迅速减小,50 cm以下土层变异系数较小且随深度变化微小;(3)不同龄阶梭梭根区剖面平均土壤含水率全年与春、夏、秋季均表现为:枯树成熟梭梭中龄梭梭裸地;(4)随距梭梭树干距离的增大(0—5 m范围内),土壤含水率整体呈减小趋势;降雨前后,梭梭根区浅层(0—10 cm)土壤含水率增量大于裸地土壤含水率增量。     

Measuring very negative water potentials with polymer tensiometers: principles,performance and applications

In recent years, a polymer tensiometer (POT) was developed and tested to directly measure matric potentials in dry soils. By extending the measurement range to wilting point (a 20-fold increase compared to conventional, water-filled tensiometers), a myriad of previously unapproachable research questions are now open to experimental exploration. Furthermore, the instrument may well allow the development of more water-efficient irrigation strategies by recording water potential rather than soil water content. The principle of the sensor is to fill it with a polymer solution instead of water, thereby building up osmotic pressure inside the sensor. A high-quality ceramic allows the exchange of water with the soil while retaining the polymer. The ceramic has pores sufficiently small to remain saturated even under very negative matric potentials. Installing the sensor in an unsaturated soil causes the high pressure of the polymer solution to drop as the water potentials in the soil and in the POT equilibrate. As long as the pressure inside the polymer chamber remains sufficiently large to prevent cavitation, the sensor will function properly. If the osmotic potential in the polymer chamber can produce a pressure of approximately 2.0 MPa when the sensor is placed in water, proper readings down to wilting point are secured. Various tests in disturbed soil, including an experiment with root water uptake, demonstrate the operation and performance of the new polymer tensiometer and illustrate how processes such as root water uptake can be studied in more detail than before. The paper discusses the available data and explores the long term perspectives offered by the instrument.     

Water sources accessed by arid zone riparian trees in highly saline environments,Australia

The flow regimes of arid zone rivers are often highly variable, and shallow groundwater in the alluvial aquifers can be very saline, thus constraining the availability and quality of the major water sources available to riparian trees—soil water, shallow groundwater and stream water. We have identified water sources and strategies used by riparian trees in more highly saline and arid conditions than previously studied for riparian trees of arid zone rivers. Our research focused on the riparian species Eucalyptus coolabah, one of the major riparian trees of ephemeral arid zone rivers in Australia. The water sources available to this riparian tree were examined using δ¹⁸O isotope data from xylem, soil water, groundwater and surface water. Additionally, soil chloride and matric potential data were used to infer zones of water availability for root uptake. Despite the saline conditions, the trees used a mixture of soil water and groundwater sources, but they did not use surface water directly. The study identified three strategies used to cope with typically high groundwater and soil water salinities. Firstly, the trees preferentially grow in zones of most frequent flushing by infiltrating streamflow, such as the bank-tops of channels. Secondly, the trees limit water use by having low transpiration rates. Thirdly, the trees are able to extract water at very low osmotic potentials, with water uptake continuing at chloride concentrations of at least 20,000–30,000 mg L⁻¹.     

Parametric studies on bioengineering effects of tree root-based suction on ground behaviour

Using native vegetation to improve soil stiffness, stabilise slopes and control erosion is a rapidly evolving process. A theoretical model previously developed by the authors for the rate of tree root water uptake together with an associated numerical simulation is used to study the effects of a wide range of soil, tree, and atmospheric parameters on partially saturated ground. The influence of different parameters on the maximum initial rate of root water uptake is investigated through parametric and sensitivity analyses. Field measurements taken from previously published literature are compared with numerical predictions for validation. The rate of selected parameters such as potential transpiration and its distribution, suction at wilting point, the coefficient of permeability and the distribution of root length density are studied in detail. The analysis shows that the rate of potential transpiration increases the soil matric suction and ground settlement, while the potential transpiration rate has an insignificant effect on the distribution of soil suction. Root density distribution factors affect the size of the influence zone. Suction at the wilting point increases the soil matric suction and ground settlement, whereas the saturation permeability decreases the maximum soil matric suction generated. The analysis confirms that the most sensitive parameters, including the coefficients of the tree root system, the transpiration rate, the permeability of the soil and its suction at the wilting point should be measured or estimated accurately for an acceptable prediction of ground conditions in the vicinity of trees.     

Modelling the effect of varying soil water on root growth dynamics of annual crops

We present a simple framework for modelling root growth and distribution with depth under varying soil water conditions. The framework considers the lateral growth of roots (proliferation) and the vertical extension of roots (root front velocity). The root front velocity is assumed to be constant when the roots descend into an initially wet soil profile. The lateral growth of roots is governed by two factors: (1) the current root mass or root length density at a given depth, and (2) soil water availability at that depth.Under non-limiting soil water conditions, the increase in root mass at any depth is governed by a logistic equation so that the root length density (R _v) cannot exceed the maximum value. The maximumR _v, is assumed to be the same for all depths. Additional dry matter partitioned to roots is initially distributed according to the current root mass at each depth. As the root mass approaches the maximum value, less dry matter is partitioned to that depth.When soil water is limiting, a water deficit factor is introduced to further modify the distribution of root dry matter. It is assumed that the plant is an energy minimiser so that more root mass is partitioned to the wetter regions of the soil where least energy will be expended for root growth. Hence, the model allows for enhanced root growth in areas where soil water is more easily available.Simulation results show that a variety of root distribution patterns can be reproduced due to varying soil water conditions. It has been demonstrated that broad patterns of root distribution reported in the literature can also be simulated by the model.     

Use of a microtensiometer technique to study hydraulic lift in a sandy soil planted with pearl millet (Pennisetum americanum [L.] Leeke)

A pot experiment was carried out with pearl millet (Pennisetum americanum [L.] Leeke) growing in a sandy soil in which the upper (topsoil) and lower (subsoil) parts of the pots were separated by a perlite layer to prevent capillary water movement. Using microtensiometers a study was made to establish whether it was possible to measure hydraulic lift by which the upper part of the soil was rewetted when water was supplied exclusively to the lower part of the soil.Hydraulic lift occurred during the first seven days of the period of measurement, with a maximum water release to the soil of 2.7 Vol. % during one night (equivalent to 10.8 mL water in the top 10 cm of the soil profile). This magnitude was obtained at very high root length densities, so that water release from the roots would be expected to be much smaller under field conditions.Hydraulic lift ceased when the soil matric potential in the topsoil dropped below-10 kPa at the end of the light period and could not be re-established, neither by extending the dark period, nor after rewatering the topsoil. The disappearance of hydraulic lift could be explained in part through osmotic adaptation of plant roots and, thus prevention of water release from the roots in the topsoil. It is concluded that hydraulic lift may affect nutrient uptake from drying topsoil by extending the time period favourable for uptake from the topsoil.     

Drip irrigation,soil characteristics and the root distribution and root activity of olive trees

A study was carried out on the root distribution and root activity of the olive tree (Olea Europaea, L., var. manzanillo) as influenced by drip irrigation and by several soil characteristics such as texture and depth. The experiments were conducted in two plots within a drip-irrigated grove of 20-year-old trees planted at 7×7 m spacing. One soil was a sandy loam, the other a clay-loam. Both cylinder and trench methods were used to determine root distribution. Labelling with ³²P was used to determine root activity. Under dryland conditions the adult tree adapted its rooting system, following the installation of a drip system, by concentrating the roots within the wet soil zones near the drippers. The highest root densities occur in those zones, down to a 0.6 m depth, the most abundant being the <0.5 mm diameter roots. The most intensive root activity was also found in that zone. For a given irrigation system, wet soil bulbs are more extensive and therefore root distribution expands to a larger soil volume when the soil is more clayey and with a hard calcareous pan present at about 0.8 m depth which prevents deep drainage.     

A coupled model of stomatal conductance, photosynthesis and transpiration

A model that couples stomatal conductance, photosynthesis, leaf energy balance and transport of water through the soil–plant–atmosphere continuum is presented. Stomatal conductance in the model depends on light, temperature and intercellular CO₂ concentration via photosynthesis and on leaf water potential, which in turn is a function of soil water potential, the rate of water flow through the soil and plant, and on xylem hydraulic resistance. Water transport from soil to roots is simulated through solution of Richards’ equation. The model captures the observed hysteresis in diurnal variations in stomatal conductance, assimilation rate and transpiration for plant canopies. Hysteresis arises because atmospheric demand for water from the leaves typically peaks in mid‐afternoon and because of uneven distribution of soil matric potentials with distance from the roots. Potentials at the root surfaces are lower than in the bulk soil, and once soil water supply starts to limit transpiration, root potentials are substantially less negative in the morning than in the afternoon. This leads to higher stomatal conductances, CO₂ assimilation and transpiration in the morning compared to later in the day. Stomatal conductance is sensitive to soil and plant hydraulic properties and to root length density only after approximately 10 d of soil drying, when supply of water by the soil to the roots becomes limiting. High atmospheric demand causes transpiration rates, LE, to decline at a slightly higher soil water content, θ_s, than at low atmospheric demand, but all curves of LE versus θ_s fall on the same line when soil water supply limits transpiration. Stomatal conductance cannot be modelled in isolation, but must be fully coupled with models of photosynthesis/respiration and the transport of water from soil, through roots, stems and leaves to the atmosphere.     

Root dynamics of Melaleuca halmaturorum in response to fluctuating saline groundwater

Melaleuca halmaturorum is a salt and waterlogging tolerant tree and thus often occurs in saline areas fringing permanent wetlands and in ephemeral swamps. The dominance of this tree in natural groundwater discharge areas may result in M. halmaturorum transpiration making a major contribution to groundwater discharge. To quantify this the seasonal changes in tree water sources in response to fluctuating soil salinity and waterlogging were examined. This study was conducted in a natural system where seasonally fluctuating saline groundwater (64 dS m^–1; 0.3–1.2 m deep) allowed the patterns of M. halmaturorum root water uptake to be followed over a 15 month period. Tree water sources were examined using the naturally occurring stable isotopes of water, while new root growth was examined using a field root observation window and from soil cores. The presence of isotopic fractionation of ²H under conditions of soil salinity and waterlogging was tested in a glasshouse experiment. Measurements of soil and leaf water potential were also made to examine the possible water sources and limits to water uptake. No isotopic fractionation was found by tree roots under conditions of salinity and waterlogging. M. halmaturorum trees were active in taking up groundwater at most times and combined this with a shallower soil water source replenished by rainfall in winter. Water uptake was concentrated in the deeper parts of the soil profile when the groundwater was at its deepest and salt had accumulated in the surface soils, at the end of summer. When groundwater rose, at the end of winter, roots responded by extracting water from near the soil surface (0–0.1 m), at the new watertable. This pattern of water uptake in response to groundwater fluctuations and salt accumulation in the surface soil was also reflected in new root tip appearance at the root observation window. Fluctuations in leaf water potential fallowed fluctuations in surface soil (0.1 m depth) water potential at all times. In winter leaf water potential reflected the absolute values of the surface soil water potential but in summer it was between surface soil and groundwater water potentials. We conclude that M. halmaturorum used groundwater in summer and a combination of rainfall and groundwater from the surface soils in winter. The ability to take up water from saline substrates through the maintenance of low leaf water potential, combined with this ability to rapidly alter root water uptake in response to changes in soil water availability contributed to the survival of M. halmaturorum in this saline swamp.