Organ | Reference | Species | B0 (T) | Highlights |
---|---|---|---|---|
Fruit | Baek et al. [35] | Solanum lycopersicum cv. Tiara, Tiara TY, and Unicorn | 1 | Variation in signal intensity as a function of maturity; Assignment of maturity based on the pericarp/locule signal ratio |
Geya et al. [52] | Pyrus pyrifolia | 0.2 | Variation in T2 as a function of fruit growth and changes in tissue structure; Linear relationship between relaxation rates and the inverse of the cube root of pear fruit weight | |
Windt and Blümler [48] | Phaseolus vulgaris L | 0.26 | Monitoring of fruit water content and fruit growth | |
Leaves | Capitani et al. [54] | Zea mays; Phaseolus vulgaris; Populus nigra; Cistus incanus; Quercus ilex | 0.4 | Relationship between the integral of the NMR signal and leaf water status, and with the rate of transpiration in hydrated leaves; Reduction in NMR signal with leaf dehydration; Different trends between species depending on their water strategies |
Musse et al. [49] | Brassica napus L., genotype Tenor | 0.47 | Access to cell structure by measuring T2 through subcellular water distribution; Variation in T2 distribution as a function of leaf developmental stage | |
Musse et al. [51] | Brassica napus L., genotype Aviso | 0.47 | Reflection of the senescence process in the variation of T2 distribution; Earlier change in T2 than in chlorophyll and dry matter content | |
Sorin et al. [50] | Brassica napus L., genotype Tenor | 0.47 | Access to cell structure by measuring T2 through subcellular water distribution; Variation in T2 distribution as a function of leaf developmental stage | |
Sorin et al. [58] | Nicotiana tabacum cv. Xanthi | 0.47 | The stage of leaf development mainly affects the longest T2; The impact of water stress depends on the plant's stage of development and the intensity of the stress | |
Windt et al. [37] | Oryza sativa cv. Nuovo Maratelli | 0.242 | Diurnal variation in leaf water content; Weaker tendency in case of osmotic stress | |
Stem | Fukuda et al. [59] | Cercidiphyllum japonicum; Betula platyphylla var. japonica | 1 | Measurement of water content; Visualization of emboli propagation; Estimation of the relative area of the embolism from MR images in accordance with vulnerability curves |
Homan et al. [39] | Prunus | 0.7 | Similar flow measurements at high and low magnetic fields | |
Jones et al. [36] | Prunus padus | 0.025 | Imaging water distribution; Correlation between signal intensity and meteorological conditions; Diurnal and seasonal variation in water status | |
Kimura et al. [11] | Pyrus pyrifolia | 0.3 | Clear difference between the ADC map of the branch affected by dwarf disease and the ADC map of the normal branch; Variation in microscopic water flow in the branch as a function of solar radiation | |
Malone et al. [56] | Populus tremuloides; Juniperus monosperma; Pinus edulis | 9E-04 | Diurnal variation of the NMR signal in a well-watered plant; No clear diurnal variation of the NMR signal in a water-limited plant | |
Meixner et al. [10] | Fagus sylvatica | 0.25 | Measurement of water content; Visualization of emboli propagation; | |
Meixner et al. [34] | Malus domestica cv. Captan; Fagus sylvatica | 0.25 | Imaging water distribution; Diurnal variation in water content and T2 | |
Nagata et al. [33] | Zelkova serrata | 0.2 | Monitoring tree growth; Diurnal and seasonal variation in xylem flow | |
Peuke et al. [62] | Ricinus communis L | 0.72 | Reduction in phloem and xylem flows during root anoxia treatment; No diurnal variation in xylem sap flow after anoxia treatment; Reduction then recovery of phloem sap flow during shoot anoxia treatment | |
Scheenen et al. [53] | Cucumis sativus cv. Hurona | 0.7 | Reduction in root water uptake and xylem hydraulic conductance due to emboli formation after cold stress; Refilling monitoring | |
Umebayashi et al. [60] | Pinus thunbergii | 0.3 | Imaging the spread of embolism in pine wilted disease caused by nematodes; Characterization of two types of embolism, one of which spread in all directions and was caused by the nematode population staying around the inoculation site | |
Utsuzawa et al. [61] | Pinus thunbergii | 1 | Visualisation of xylem cavitation and the spread of embolism caused by nematodes; Area and speed of cavitation spreading in two stages: a first one with gradual and confined propagation, and second, rapid propagation progressing until it occupied most of the xylem | |
Van As et al. [40] | Cucumis sativus L | 0.235 | Variation in flux and T2 with light intensity | |
Windt et al. [12] | Populus tremula × Populus alba, INRA clone 717 1B4; Ricinus communis; Lycopersicon esculentum cv. Counter; Nicotiana tabacum cv. Petit Havana SR1 | 0.72 | Measurement of phloem and xylem flow; Diurnal variation in xylem flow | |
Windt et al. [47] | Ricinus communis; Populus nigra | 0.57 | Non spatially resolved xylem flow measurement; Diurnal variation in water status; Monitoring the growth of a tree trunk | |
Windt and Blümler [48] | Populus nigra L.; Quercus robur L | 0.57 0.26 | Measurement of xylem flow; Monitoring water content, stem diameter growth and shrinkage | |
Yoder et al. [55] | Populus tremuloides; Pinus edulis; Juniperus monosperma; Pinus ponderosa | 9E-04 | Decrease in signal amplitude as the tree dries out | |
Roots | Bagnall et al. [38] | Sorghum bicolor (L. Moench) | 0.047 | Measuring soil and root T2; Soil T2 variation as a function of soil type; Imaging roots in the soil |
Bagnall et al. [13] | Sorghum bicolor (L. Moench) | 0.047 | 2D and 3D imaging of root architecture in soils; Root segmentation | |
Nuixe et al. [46] | Dactylis glomerata; Plantago lanceolata; Medicago sativa | 0.3 | Diurnal variation in water content and in T2 |