Geographic isolates of Glomus increase root growth and whole-plant transpiration of Citrus seedlings grown with high phosphorus

Mycorrhiza ◽  
2001 ◽  
Vol 10 (5) ◽  
pp. 231-236 ◽  
Author(s):  
Matthew W. Fidelibus ◽  
C. A. Martin ◽  
Jean C. Stutz
2019 ◽  
Vol 46 (12) ◽  
pp. 1072 ◽  
Author(s):  
Geetika Geetika ◽  
Erik J. van Oosterom ◽  
Barbara George-Jaeggli ◽  
Miranda Y. Mortlock ◽  
Kurt S. Deifel ◽  
...  

Water scarcity can limit sorghum (Sorghum bicolor (L.) Moench) production in dryland agriculture, but increased whole-plant transpiration efficiency (TEwp, biomass production per unit of water transpired) can enhance grain yield in such conditions. The objectives of this study were to quantify variation in TEwp for 27 sorghum genotypes and explore the linkages of this variation to responses of the underpinning leaf-level processes to environmental conditions. Individual plants were grown in large lysimeters in two well-watered experiments. Whole-plant transpiration per unit of green leaf area (TGLA) was monitored continuously and stomatal conductance and maximum photosynthetic capacity were measured during sunny conditions on recently expanded leaves. Leaf chlorophyll measurements of the upper five leaves of the main shoot were conducted during early grain filling. TEwp was determined at harvest. The results showed that diurnal patterns in TGLA were determined by vapour pressure deficit (VPD) and by the response of whole-plant conductance to radiation and VPD. Significant genotypic variation in the response of TGLA to VPD occurred and was related to genotypic differences in stomatal conductance. However, variation in TGLA explained only part of the variation in TEwp, with some of the residual variation explained by leaf chlorophyll readings, which were a reflection of photosynthetic capacity. Genotypes with different genetic background often differed in TEwp, TGLA and leaf chlorophyll, indicating potential differences in photosynthetic capacity among these groups. Observed differences in TEwp and its component traits can affect adaptation to drought stress.


2019 ◽  
Vol 32 (1) ◽  
pp. 86-94 ◽  
Author(s):  
Nicolás M. Cecchini ◽  
Suruchi Roychoudhry ◽  
DeQuantarius J. Speed ◽  
Kevin Steffes ◽  
Arjun Tambe ◽  
...  

Local interactions between individual plant organs and diverse microorganisms can lead to whole plant immunity via the mobilization of defense signals. One such signal is the plastid lipid-derived oxylipin azelaic acid (AZA). Arabidopsis lacking AZI1 or EARLI1, related lipid transfer family proteins, exhibit reduced AZA transport among leaves and cannot mount systemic immunity. AZA has been detected in roots as well as leaves. Therefore, the present study addresses the effects on plants of AZA application to roots. AZA but not the structurally related suberic acid inhibits root growth when directly in contact with roots. Treatment of roots with AZA also induces resistance to Pseudomonas syringae in aerial tissues. These effects of AZA on root growth and disease resistance depend, at least partially, on AZI1 and EARLI1. AZI1 in roots localizes to plastids, similar to its known location in leaves. Interestingly, kinases previously shown to modify AZI1 in vitro, MPK3 and MPK6, are also needed for AZA-induced root-growth inhibition and aboveground immunity. Finally, deuterium-labeled AZA applied to the roots does not move to aerial tissues. Thus, AZA application to roots triggers systemic immunity through an AZI1/EARLI1/MPK3/MPK6-dependent pathway and AZA effects may involve one or more additional mobile signals.


2020 ◽  
Vol 12 (24) ◽  
pp. 4070
Author(s):  
Florian Ellsäßer ◽  
Alexander Röll ◽  
Joyson Ahongshangbam ◽  
Pierre-André Waite ◽  
Hendrayanto ◽  
...  

Plant transpiration is a key element in the hydrological cycle. Widely used methods for its assessment comprise sap flux techniques for whole-plant transpiration and porometry for leaf stomatal conductance. Recently emerging approaches based on surface temperatures and a wide range of machine learning techniques offer new possibilities to quantify transpiration. The focus of this study was to predict sap flux and leaf stomatal conductance based on drone-recorded and meteorological data and compare these predictions with in-situ measured transpiration. To build the prediction models, we applied classical statistical approaches and machine learning algorithms. The field work was conducted in an oil palm agroforest in lowland Sumatra. Random forest predictions yielded the highest congruence with measured sap flux (r2 = 0.87 for trees and r2 = 0.58 for palms) and confidence intervals for intercept and slope of a Passing-Bablok regression suggest interchangeability of the methods. Differences in model performance are indicated when predicting different tree species. Predictions for stomatal conductance were less congruent for all prediction methods, likely due to spatial and temporal offsets of the measurements. Overall, the applied drone and modelling scheme predicts whole-plant transpiration with high accuracy. We conclude that there is large potential in machine learning approaches for ecological applications such as predicting transpiration.


2004 ◽  
Vol 31 (9) ◽  
pp. 903 ◽  
Author(s):  
Ian C. Dodd ◽  
Chuong Ngo ◽  
Colin G. N. Turnbull ◽  
Christine A. Beveridge

The rms2 and rms4 pea (Pisum sativum L.) branching mutants have higher and lower xylem-cytokinin concentration, respectively, relative to wild type (WT) plants. These genotypes were grown at two levels of nitrogen (N) supply for 18–20 d to determine whether or not xylem-cytokinin concentration (X-CK) or delivery altered the transpiration and leaf growth responses to N deprivation. Xylem sap was collected by pressurising de-topped root systems. As sap-flow rate increased, X-CK declined in WT and rms2, but did not change in rms4. When grown at 5.0 mm N, X-CKs of rms2 and rms4 were 36% higher and 6-fold lower, respectively, than WT at sap-flow rates equivalent to whole-plant transpiration. Photoperiod cytokinin (CK) delivery rates (the product of transpiration and X-CK) decreased more than 6-fold in rms4. Growth of plants at 0.5 mm N had negligible (< 10%) effects on transpiration rates expressed on a leaf area basis in WT and rms4, but decreased transpiration rates of rms2. The low-N treatment decreased leaf expansion by 20–25% and expanding leaflet N concentration by 15%. These changes were similar in all genotypes. At sap-flow rates equivalent to whole-plant transpiration, the low N treatment decreased X-CK in rms2 but had no discernible effect in WT and rms4. Since the low N treatment decreased transpiration of all genotypes, photoperiod CK delivery rates also decreased in all genotypes. The similar leaf growth response of all genotypes to N deprivation despite differences in both absolute and relative X-CKs and deliveries suggests that shoot N status is more important in regulating leaf expansion than xylem-supplied cytokinins. The decreased X-CK and transpiration rate of rms2 following N deprivation suggests that changes in xylem-supplied CKs may modify water use.


2006 ◽  
Vol 57 (7) ◽  
pp. 761 ◽  
Author(s):  
Eun-Young Choi ◽  
Ann McNeill ◽  
David Coventry ◽  
James Stangoulis

Within the semi-arid region of south-eastern Australia, high levels of subsoil boron (B) in alkaline soil can limit production of dryland crops. The aim of this research was to investigate the whole plant response to a range of subsoil-extractable B concentrations for a number of crop and weed species common to agricultural areas of South Australia. Specifically, the objectives were to determine (a) the morphological response of the entire root system to high subsoil B and (b) the available B concentrations in subsoil critical for expression of shoot traits commonly used in selection of B tolerance. Barley grass (Hordeum glaucum L.), crop barley (Hordeum vulgare) variety Clipper and breeders’ line VB9953, fababean (Vicia faba var. Fjiord), Lincoln weed (Diplotaxis tenuifolia L.), prickly lettuce (Lactuca serriola), and evening primrose (Oenothera stricta L.) were grown in sealed PVC cylinders (500 mm deep by 150 mm diam.) containing a sandy soil. The concentration of extractable B in the topsoil (0–0.20 m), considered non-toxic, was 0.5 mg/kg for all cylinders but a range of B treatments (0.5, 2.4, 4.3, 6.8, or 12.2 mg/kg) was applied directly to the subsoil (0.30–0.50 m). Increasing the concentration of extractable B in the subsoil decreased root dry weight in this region, but did not reduce water use from subsoil by barley grass or evening primrose. The response of the roots in the topsoil and subsequent responses in the shoot also differed among species. Symptoms of B toxicity in shoots of all the species were observed at subsoil-extractable B concentrations of 12.2 mg/kg and at lower concentrations in some of the crop and weed species. Shoot growth, total water use, and root growth in topsoil of Clipper and Lincoln weed were severely impaired by high subsoil-extractable B, as was topsoil root growth in evening primrose, with the reduction in the weed species being mostly associated with a decrease in taproot dry weight. Barley grass, VB9953, evening primrose, and to a lesser extent fababean and prickly lettuce, maintained shoot growth at all subsoil-extractable B concentrations, despite a reduction in subsoil water use by VB9953. Prickly lettuce and VB9953 also sustained root growth in the topsoil whilst fababean and barley grass increased root growth in the topsoil in response to high subsoil extractable B. There was no direct relationship between the quantity of B accumulated in shoots and detrimental effects on growth. Furthermore, there appeared to be no direct relationship between water uptake and B uptake since irrespective of the effect of subsoil B on either subsoil or total water use, shoot B concentration increased in all the species/genotypes as subsoil B increased. The degree to which plants were deemed to exhibit tolerance was, therefore, highly dependent upon the trait used for assessment. One suggestion in the current study is that shoot dry matter in B toxic soil can be a consistent parameter for considering varieties for tolerance to B toxicity.


2014 ◽  
Vol 41 (1) ◽  
pp. 1 ◽  
Author(s):  
M. F. Arndal ◽  
I. K. Schmidt ◽  
J. Kongstad ◽  
C. Beier ◽  
A. Michelsen

Ecosystems exposed to elevated CO2 are often found to sequester more atmospheric carbon due to increased plant growth. We exposed a Danish heath ecosystem to elevated CO2, elevated temperature and extended summer drought alone and in all combinations in order to study whether the expected increased growth would be matched by an increase in root nutrient uptake of NH4+-N and NO3– -N. Root growth was significantly increased by elevated CO2. The roots, however, did not fully compensate for the higher growth with a similar increase in nitrogen uptake per unit of root mass. Hence the nitrogen concentration in roots was decreased in elevated CO2, whereas the biomass N pool was unchanged or even increased. The higher net root production in elevated CO2 might be a strategy for the plants to cope with increased nutrient demand leading to a long-term increase in N uptake on a whole-plant basis. Drought reduced grass root biomass and N uptake, especially when combined with warming, but CO2 was the most pronounced main factor effect. Several significant interactions of the treatments were found, which indicates that the responses were nonadditive and that changes to multiple environmental changes cannot be predicted from single-factor responses alone.


1986 ◽  
Vol 13 (1) ◽  
pp. 143 ◽  
Author(s):  
R Munns ◽  
A Termaat

This paper discusses whole-plant responses to salinity in order to answer the question of what process limits growth of non-halophytes in saline soils. Leaf growth is more sensitive to salinity than root growth, so we focus on the process or processes that might limit leaf expansion. Effects of short-term exposure (days) are considered separately from long-term exposure (weeks to years). The answer in the short term is probably the water status of the root and we suggest that a message from the root is regulating leaf expansion. The answer to what limits growth in the long term may be the maximum salt concentration tolerated by the fully expanded leaves of the shoot; if the rate of leaf death approaches the rate of new leaf expansion, the photosynthetic area will eventually become too low to support continued growth.


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