Responses of tomato (Solanum lycopersicum L.) plants to iron deficiency in the root zone

Published by the Polish Society for Horticultural Science since 1989 Folia Hort. 31(1) (2019): 223-234 Folia Horticulturae DOI: 10.2478/fhort-2019-0017 http://www.foliahort.ogr.ur.krakow.plORIGINAL ARTICLE Open access ABSTRACT Iron deficiency induces a yellowing in the aerial part of plants, known as iron chlorosis, and reduces the growth, yield, and quality of the fruits. Understanding plant response to iron deficiency is essential for agronomic management. This study decoded the temporal response of tomato plants (Solanum lycopersicum L.) to iron deficiency by quantifying different vegetative parameters. Subapical root swelling in the first 2.0 mm and several shoot and root growth parameters were measured in plants grown in a nutrient solution with and without Fe, on different dates designated as days after transplantation (DAT). Correlations between the total chlorophyll concentration in young leaves and 22 morphological and physiological parameters were also calculated. The plants grown in the absence of Fe had a higher number of secondary roots at 3 DAT, compared to control plants. On the same date, subapical root swelling was also observed, particularly at 1.5 and 2.0 mm from the root tip. Those plants also had a lower chlorophyll content in young leaves and a higher ferric-chelate reductase activity (FCR; EC 1.16.1.17) in the roots. At 9 DAT, the overall vegetative performance (plant height, fresh weight of stems and leaves) was negatively affected. At the end of the experiment (14 DAT), significant correlations were found between chlorophyll and the studied parameters. In conclusion, tomato plants experienced a cascade of responses to Fe deficiency throughout nine days: firstly, root lateralization increased; later, root swelling was observed, and a decrease in leaf chlorophyll content was registered associated with an increase in root FCR. At the end, the biomass of tomato plants decreased. Key words: chlorophyll, ferric-chelate reductase (FCR), plant nutrition, root lateralization, stress physiology, subapical root swelling Abbreviations: Chl – chlorophyll, DAT – days after transplantation, DW – dry weight, FCR – ferric-chelate reductase, Fe0 – Fe deficient, Fe10 – Fe sufficient, FW – fresh weight, PPFD – photosynthetic photon flux density, R/S – roots/upper part of the tomato plants Responses of tomato (Solanum lycopersicum L.) plants to iron deficiency in the root zone María Rocío Jiménez1*, Laura Casanova1, Teresa Saavedra2, Florinda Gama2, María Paz Suárez1, Pedro José Correia2, Maribela Pestana2 1 Departamento de Ciencias Agroforestales, ETSIA, Universidad de Sevilla Carretera de Utrera, km 1, 41013 Sevilla, Spain 2 MeditBio-Center for Mediterranean Bioresources and Food, University of Algarve FCT, Ed8, Campus of Gambelas, 8005-139, Faro, Portugal *Corresponding author. e-mail: [email protected] (M.R. Jiménez). INTRODUCTION Understanding the mechanisms of Fe uptake, trafficking and homeostasis that occur both at the cellular level and whole plant level is essential to improve the quality and productivity of agricultural crops, and it contributes to healthier and improved Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC 224 Responses to iron deficiency world food supplies. Since Fe is both essential and noxious to plant metabolism, the concentration and distribution of Fe to various organs and tissues must be tightly balanced within the physiological limits to provide the adequate amounts of Fe required for metabolic processes and plant survival (Guerinot and Yi, 1994). The regulation of Fe uptake is an initial process that is essential for maintaining Fe homeostasis in plants. In Fe-limiting conditions, higher plants have developed two strategies to facilitate Fe acquisition. These strategies were first described by Römheld and Marschner (1986) and are known as strategy I and strategy II. Strategy I (known as the reduction strategy) is based on the reduction of Fe(III) to Fe(II) before uptake via membrane-bound ferric-chelate reductase (FCR, belonging to the FRO (Ferric Reduction Oxidase) family of genes). This strategy is used by nongrass species such as Arabidopsis (Arabidopsis thaliana L. Heynh). The tomato plant (Solanum lycopersicum L.) is also broadly used as a model species for investigating this strategy (Zuchi et al., 2009; Paolacci et al., 2014). The deprivation of Fe in plant tissues leads to a significantly reduced chlorophyll content in the leaves (Álvarez-Fernández et al., 2011). The characteristic yellow colour of chlorosis that occurs in young leaves is a result of a relative enrichment with carotenoids (Morales et al., 1990). Roots are also affected. Contrary to what happens under low pH (< 5.0) conditions, which significantly decrease root growth (Graças et al., 2016), iron deficiency causes morphological modifications manifested as an increase in the number of secondary roots associated with root hair formation and root tip swelling, both of which aim to cover a greater area in the rhizosphere in the search for Fe (Pestana et al., 2012). Lateral root elongation is dependent on the auxin influx transporter (AUX1) that accumulates the growth substance auxin in newly formed lateral root tips (Giehl et al., 2012). In a study performed on Arabidopsis, the aha7 mutant showed significantly fewer root hairs, suggesting a contribution of AHA7 in the differentiation of rhizodermic cells (Santi and Schmidt, 2009). In Malus spp. grown in a root-split system, it was found that the Feinduced physiological responses were mediated by systematic auxin signalling from shoots to roots (Wu et al., 2012). Although some important work has been done to understand the physiological mechanisms involved in the response to iron deficiency, such as hormonal regulation (Landsberg, 1995) or ethylene participation (Romera and Alcántara, 2004; Lucena et al., 2015), external morphology traits such as subapical root swelling has not yet been quantified in any species. To our knowledge, it has only been qualitatively described in some crops such as orange and carob trees (Pestana et al., 2001; Correia et al., 2003). Understanding subapical root swelling may reveal the location and speed of the responses to Fe deprivation. The aim of this research was to study with precision the temporal response of tomato plants to iron deficiency on different days after transplantation (DAT) by means of 22 quantitative parameters related to overall plant growth, root morphology and physiology, and chlorophyll content in the leaves. MATERIAL AND METHODS Plant culture Plants of tomato (Solanum lycopersicum L.) cv. Roma presenting two fully expanded leaves and obtained from a commercial nursery were sterilised by immersion for 24 h in a solution with 1.33 g L-1 of fosetyl-aluminium and then washed thoroughly in running water. The plants were placed in 20-L plastic containers filled with Hoagland’s nutrient solution: 5 mM Ca(NO3)2, 5 mM KNO3, 1 mM KH2PO4, 2 mM MgSO4, 46 µM H3BO3, 0.8 µM ZnSO4, 0.4 µM CuSO4, 9 µM MnCl2, and 0.02 µM MoO3, containing either 10 µM Fe (Fe10, added as Fe(III)- FeEDDHA, control plants) or no Fe (Fe0). The initial pH of the hydroponic medium was adjusted with NaOH (1 M) to 6.0 ± 0.1, and the electrical conductivity (EC, 2.2 ± 0.1 dS m-1) was assessed daily. The solutions were constantly aerated using an air pump and a diffusion system. Plants were maintained in a glasshouse under natural photoperiod conditions: a photosynthetic photon flux density (PPFD) of 150-450 µmol m-2 s-1, and the temperature ranged between 20 and 25°C, values that are normally registered in the Mediterranean region during spring. The experimental layout was a randomized design with 6 plants per treatment (Fe0 (Fedeficient) and Fe10 (Fe-sufficient)), with three replicates, and 4 sampling dates (3, 6, 9 and 14 days after transplantation (DAT)), with a total of 144 tomato plants (6 plants per container and a total of 24 containers). At the beginning of the experiment (0 DAT), a set of another fifteen (five per replicate) plants was used for general plant characterization. Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC M.R. Jiménez, L. Casanova, T. Saavedra, F. Gama, M.P. Suárez, P.J. Correia, M. Pestana 225 On each date, five plants from each treatment and replicate were separated into roots, stems, young leaves and mature leaves, and one plant was used to determine the volume of the whole root system (mL). Assessment of total leaf chlorophyll concentration The total leaf chlorophyll (Chl) concentration per unit area (µmol m-2) was estimated nondestructively using a SPAD-502 Chlorophyll Meter (Minolta Camera Co., Osaka, Japan). A calibration curve had previously been established between SPAD values and Chl concentration by extracting pigments from leaves with different degrees of chlorosis, from the same area where SPAD readings had been taken. Pigment extraction was done with pure acetone in the presence of Na ascorbate (Abadía and Abadía, 1993), and the total leaf chlorophyll (Chl) concentration per unit area (µmol m-2) was measured spectrophotometrically. The Lichtenthaler (1987) equations were used to estimate Chl, and a general linear model: (y = b0 + b1x) was fitted between SPAD values and total Chl concentration (µmol m-2) (Fig. 1). SPAD readings were taken on one mature basal leaf and on one fully expanded new leaf (apical leaf) of six plants per treatment and replicate at least five times a week. The evolution of the decrease in the total leaf chlorophyll concentration per unit area (ΔChl, µmol m-2) between the Fe treatments (Fe-deficient (Fe0) and Fe-sufficient (Fe10)) was calculated for each date using the following equation: ΔChl = ChlFe0 - ChlFe10 Evaluation of root swelling Root system On each date, the whole root system of a plant was examined in each treatment and replicate. The volume of the entire root system (mL) was determined from the volume of water displaced by immersing the roots in a test tube with a 100mL capacity. Five roots of these plants per date, treatment and replicate were selected, and the degree of swelling was determined by classifying the roots into four categories according to a methodology previously established by our group: category 0 (no root swelling; S0), category 1 (root swelling in the first quarter of its length at the root tip; S1), category 2 (root swelling up to half its length; S2), and category 3 (more than half the root had swelled; S3). Additionally, in the same plants, the number of roots with secondary roots in the first 2.0 cm from the root tip was quantified to calculate root lateralization, defined as the percentage (%) of roots with secondary roots in the first 2.0 cm of their length. Root segments Ten apical root segments (with a length of approximately 2.0 cm) per date, treatment, and replicate were taken and maintained by immersion in distilled water to avoid dehydration. Then, the root tips were fixed in an FAE solution (formalin, acetic acid, 95% ethanol and distilled water 10:5:50:35 v/v/v/v) according to Berlyn and Miksche (1976). Photographic images of all the root segments were taken with a Nikon digital camera (Digital Sight DS-Ri1) connected to a Nikon binocular loupe (SMZ 1270, Tokyo, Japan). Nis-Elements AR version 3.2 software was used to obtain the root Figure 1. Calibration curve between SPAD values and total leaf Chl concentration (μmol m-2) in tomato plants Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC 226 Responses to iron deficiency diameter measurements. Subapical root swelling was calculated as the difference between the diameter (µm) of the Fe0-treatment (Fe-deficient) roots and the Fe10-treatment (Fe-sufficient) roots at different distances from the root tip: 0.5, 1.0, 1.5, and 2.0 mm. A square grid (0.5 mm x 0.5 mm) (Fig. 2) was used to measure the cross-distance using NISElements AR 3.2. Determination of Fe reduction The activity of ferric-chelate reductase (FCR; EC 1.16.1.17) was measured in a root tip in five plants per each date, treatment, and replicate, through the formation of a red Fe(II)-(BPDS)3 complex according to the methodology of Bienfait et al. (1983). A root tip (with a length of approximately 2.0 cm) of each plant was incubated in the dark for one hour in an Eppendorf tube (2 mL) with 900 µL of micronutrient-free half-strength Hoagland’s nutrient solution containing 300 µM BPDS, 500 µM Fe(III)- EDTA and 5 mM MES buffer, at pH 6.0. Blank controls without plant material (extinction coefficient of 22.14 mM cm-1) were also used to correct for any unspecific Fe reduction. All readings of FCR activity (nmol Fe(II) min-1 g-1) were calculated on the basis of the fresh weight (FW, g) of roots. Biomass On each date, five tomato plants per treatment and replicate were separated into roots, stem, mature leaves and young leaves. The samples were washed with a non-ionic detergent (0.1%) to remove surface contamination, then washed with tap water, and finally rinsed three times with deionised water. The fresh weight (FW, g) was determined for each collected sample, and the dry weight (DW, g) was estimated after drying at 60°C for at least 48 h until the samples had reached a constant weight. Statistical analysis An analysis of variance (ANOVA, F test) and Duncan’s Multiple Range Test (DMRT) at p < 0.05 (IBM SPSS® software version 20) were used to discriminate significant differences among the mean values. Pearson’s correlation coefficients (r) between the total leaf chlorophyll (Chl) concentration per unit area (µmol m-2) of young leaves (dependent variable) and each of the 22 morphological and physiological parameters were also determined. RESULTS Effect of iron deficiency in leaves Typical interveinal chlorosis of young leaves started at 6 DAT and became increasingly pronounced until the end of the experiment (14 DAT), while the control plants remained green. From 6 DAT, the SPAD values in young leaves were significantly different between the treatments (Tab. 1). However, in mature leaves, significant differences were observed only after day 7. Figure 3 shows the evolution of the decrease in the total leaf chlorophyll concentration per unit area (ΔChl, µmol m-2) during the experiment, where each point represents the difference between the chlorophyll values of the Fe0 and Fe10 treatments. After transplantation, the decrease in chlorophyll was more marked in young leaves than in mature leaves, and it was significant starting from 7 DAT. As expected, at the end of the experiment, the Figure 2. Square grid used to measure the root diameter at different distances (0.5, 1.0, 1.5, and 2.0 mm) from the root tip Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC M.R. Jiménez, L. Casanova, T. Saavedra, F. Gama, M.P. Suárez, P.J. Correia, M. Pestana 227 extent of iron chlorosis was greater in young leaves (ΔChl = -858.35 µmol m-2) than in mature leaves (ΔChl = -394.67 µmol m-2). Effect of iron deficiency on roots The plants grown without Fe presented root hairs and a subapical root swelling, compared to the Fe10 (Fe-sufficient) plants, which did not show such alteration (Fig. 4A). Secondary roots were also observed on the roots of chlorotic plants, with more found in the Fe0 treatment than in the Fe10 treatment. With respect to the classification according to the degree of root swelling, the root system of the tomato plants grown with Fe (control plants, Fe10) was classified as category 0 (S0), regardless of the date. At 3 DAT, 63.3% of the roots in the Fe0 treatment did not display any swelling (category 0), and 36.7% of the roots presented a swelling classified as category 1. At 6 DAT, 90.0% of the roots presented a swelling classified as category 1 (S1), 6.7% were classified as category 2 (S2), and only 3.3% did not show any swelling (category 0; S0). On the last date, at 14 DAT, the entire root system showed signs of swelling: 56.7% of the roots presented a swelling classified as category 1 (S1), 33.3% as category 2 (S2) and 10.0% as category 3 (S3). The root diameters (µm) at different distances (0.5, 1.0, 1.5 and 2.0 mm) from the root tip, for each treatment and at 0, 3, 6, 9 and 14 DAT, are shown in Table 2. Significant differences in root diameter, higher in Fe-deficient (Fe0) with respect to Fe-sufficient (Fe10), were observed between the treatments after 6 DAT for all the distances (439.39 and 334.49 µm for 0.5 mm; 559.31 and 387.36 µm for 1 mm; 715.80 and 398.50 µm for 1.5 mm; 799.04 and 406.18 µm for 2.0 mm, respectively). In the absence of Fe (Fe0 treatment), the root diameter increased 2-4 times at all the distances (0.5, 1.0, 1.5 and 2.0 mm) from the beginning of the Table 1. Mean values of SPAD in young and mature tomato leaves according to the Fe level (n = 18) *DAT Young leaves Mature leaves Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) 0 34.75 a 34.75 a 36.19 a 36.19 a 1 37.49 a 37.70 a 37.09 a 37.66 a 2 40.73 a 40.40 a 38.93 a 38.81 a 3 41.13 a 41.46 a 36.52 a 36.95 a 6 42.06 b 37.21 a 38.76 a 37.06 a 7 41.08 b 28.34 a 39.80 b 35.89 a 8 39.91 b 24.62 a* 38.96 b 35.67 a 9 36.64 b 16.59 a 41.45 b 35.74 a 10 41.35 b 14.78 a 43.78 b 35.97 a 12 36.86 b 10.86 a 42.28 b 34.23 a 14 35.89 b 11.72 a 42.23 b 31.99 a *DAT: days after transplantation Mean values followed by different lower-case letters (a, b) in the same row indicate significant differences for each Fe treatment for young and mature leaves. The asterisk (*) indicates the date on which differences between the treatments were visually observed Figure 3. Evolution of the decrease in the total leaf chlorophyll concentration per unit area (ΔChl, μmol m-2) during the experiment, where each point represents the difference between the chlorophyll values of the Fe0 and Fe10 treatments. Different lower-case letters at each curve indicate significant differences between DAT for young and mature leaves (p < 0.05) (n = 18) Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC 228 Responses to iron deficiency experiment until 14 DAT. In the Fe10 treatment, the root diameter also increased, although to a lesser extent (1.2-1.5 times), after 9 DAT, and the increase was significant at the distances of 0.5, 1.0 and 1.5 mm (Tab. 2). Subapical root swelling was calculated as the difference between the diameter (µm) of the Fe0 roots and that of the Fe10 roots for each date. After that difference had been plotted against DAT (Fig. 4B), pronounced root swelling was observed in the 1.5-2.0 mm segment, particularly from 6 DAT onwards. However, as iron deficiency develops over time, root swelling eventually occurred at all the set distances. Root lateralization (percentage (%) of roots with secondary roots in the first 2.0 cm from the root tip) significantly increased in Fe0 (Fe-deficient) plants compared with Fe10 (Fe-sufficient) plants at 3 DAT (80% and 26.70%, respectively) and 9 DAT (80% and 3.0%, respectively) (Fig. 5A). The ferric-chelate reductase (FCR) activity (nmol Fe(II) min-1 g-1 FW) increased significantly in the roots of plants grown under Fe-deficiency compared to control plants from 6 DAT (8.90 and 2.30 nmol Fe(II) min-1 g-1 FW, respectively) until the end of the study (14 DAT; 17.60 and 2.70 nmol Fe(II) min-1 g-1 FW, respectively) (Fig. 5B). Figure 5. Root lateralization (percentage (%) of roots with secondary roots in the first 2.0 cm from the root tip; n = 15; Fig. 5A) and root ferric-chelate reductase (FCR) activity (nmol Fe(II) min-1 g-1 FW measured on different days after transplantation; n = 15; Fig. 5B). Different lower-case letters (a, b) indicate significant differences for each Fe treatment and days after transplantation (p < 0.05). Vertical bars represent ± SD Figure 4. Root segments observed under a Nikon binocular microscope, with a subapical root swelling in the Fedeficient (Fe0) treatment and no such alteration in the Fe-sufficient (Fe10) treatment. → indicates the formation of root hairs (Fig. 4A). Progress of subapical root swelling (diameter Fe0 (μm) – diameter Fe10 (μm)) after transplantation measured at different distances from the root tip (n = 30) (Fig. 4B) Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC M.R. Jiménez, L. Casanova, T. Saavedra, F. Gama, M.P. Suárez, P.J. Correia, M. Pestana 229 Table 2. Root diameter (µm) measured at different distances from the root tip in tomato plants grown in Fe-sufficient (Fe10) and Fe-deficient (Fe0) conditions on different days after transplantation (n = 30) Distance from root tip (mm) *DAT 0.5 1.0 1.5 2.0 Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) 0 310.88 aA 310.88 aA 365.71 aA 365.71 aA 376.26 aA 376.26 aA 420.45 aA 420.45 aA 3 323.92 aAB 325.69 aA 377.02 aA 373.38 aA 395.85 aA 433.79 aA 429.40 aA 402.89 aA 6 334.49 aAB 439.39 bB 387.36 aA 559.31 bB 398.50 aA 715.80 bB 406.18 aA 799.04 bB 9 383.44 aB 491.99 bB 459.13 aB 636.75 bB 480.57 aB 724.67 bB 484.90 aA 799.71 bB 14 375.95 aB 715.38 bC 462.34 aB 1135.48 bC 482.11 aB 1379.34 bC 492.18 aA 1561.47 bC *DAT: days after transplantation; Mean values followed by different lower-case letters (a, b) in the same row for each DAT and each distance indicate significant differences between the Fe treatments (p < 0.05); Mean values followed by different upper-case letters (A, B) in the same column for each Fe treatment and distance indicate significant differences among DAT (p < 0.05) Table 3. Biomass of roots, stems, young leaves (YL), mature leaves (ML), plants (number of leaves (NL) and height), and roots/upper part of tomato plants (R/S) for the two treatments (Fe-deficient (Fe0) and Fe-sufficient (Fe10)) on different days after transplantation (3, 6, 9, and 14) (n = 15). The results are the mean values 3 DAT*6 DAT 9 DAT 14 DAT Parameters Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) Fe-sufficient (Fe10) Fe-deficient (Fe0) Roots Volume (ml) 0.83 a 0.80 a 1.50 b 0.77 a 3.47 b 2.17 a 3.77 b 1.12 a FW** (g) 0.74 a 0.80 a 0.97 a 0.75 a 2.22 b 1.57 a 3.91 b 0.93 a DW*** (g) 0.04 a 0.05 a 0.05 a 0.04 a 0.10 b 0.08 a 0.16 b 0.06 a Stem Ø****(mm) 2.84 a 2.87 a 3.22 a 3.36 a 3.92 b 3.27 a 5.18 b 3.72 a FW (g) 0.44 a 0.44 a 0.61 a 0.55 a 1.74 b 1.02 a 4.10 b 1.20 a DW (g) 0.03 a 0.03 a 0.03 a 0.04 a 0.09 b 0.07 a 0.16 b 0.08 a YL FW (g) 0.31 a 0.31 a 0.51 b 0.33 a 0.86 b 0.51 a 1.80 b 0.75 a DW (g) 0.02 a 0.03 a 0.03 a 0.03 a 0.07 a 0.05 a 0.12 b 0.08 a ML FW (g) 0.30 b 0.20 a 0.70 a 0.70 a 2.70 b 1.00 a 6.30 b 1.20 a DW (g) 0.03 a 0.03 a 0.05 a 0.07 a 0.18 b 0.09 a 0.40 b 0.06 a Plants NL***** 3.20 a 3.23 a 4.40 a 4.00 a 5.00 b 4.00 a 7.40 b 5.50 a Height (cm) 12.70 a 11.70 a 14.50 b 13.30 a 12.70 b 9.70 a 29.70 b 14.40 a R/S FW (g) 0.74 a 0.77 a 0.52 a 0.47 a 0.41 a 0.58 b 0.31 a 0.33 a DW (g) 0.51 a 0.52 a 0.38 a 0.35 a 0.31 a 0.42 b 0.23 a 0.24 a *DAT: days after transplantation; **FW: fresh weight (g); ***DW: dry weight (g); ****Ø: stem diameter (mm), and *****NL: number of leaves. Mean values followed by different lower-case letters (a, b) in the same row for each parameter and DAT indicate significant differences between Fe treatments (p < 0.05) Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC 230 Responses to iron deficiency Effect of iron deficiency on biomass The fresh weight (FW) of mature leaves was significantly different between the Fe treatments three days after transplantation (3 DAT; Tab. 3). Six days after transplantation (6 DAT), significant differences were observed in the volume of roots (mL), FW of young leaves, and plant height. At 9 DAT, significant differences between the treatments were found for all the parameters except the dry weight (DW) of young leaves. At the end of the study (14 DAT), significant differences between the treatments were also found for all the parameters studied, except the roots/upper part of the tomato plants (R/S) (FW and DW). In all the parameters for which the difference exhibited statistical significance, the values obtained in the Fe0 treatment were significantly lower than those in Fe10, except for the parameter R/S at 9 DAT. Relationship between total chlorophyll concentration in young leaves and several parameters Pearson’s correlation coefficients (r) for the total leaf chlorophyll (Chl) concentration per unit area (µmol m-2) of young leaves versus each of the 22 morphological and physiological parameters at different DAT were calculated. Table 4 shows only the significant correlations, which are presented in a descending order. The total chlorophyll concentration in young leaves was strongly correlated with the vegetative parameters (e.g., height, fresh weight of mature leaves and stems (FW)) determined at the end of the experiment (9 and 14 DAT), when severe chlorosis was evident. On those dates, lower Chl was also related to greater swelling, which is expressed by the negative sign of r. Three days after transplantation (latent chlorosis), the Chl of young leaves was positively correlated with FW (r = 0.58) and Chl (r = 0.49) of mature leaves. The activity of FCR in the roots (nmol Fe(II) min-1 g-1 FW) was strongly correlated at the end of the experiment (14 DAT). Surprisingly, at 6 DAT, no significant correlations were found. DISCUSSION The effect of Fe deficiency on root morphological traits is well documented in several species (Schmidt, 1999; Hindt and Guerinot, 2012). These changes include root swelling, the formation of new root tips and root hairs, and the formation of transfer cells (e.g. Pestana et al., 2004). However, it remains an open question whether those alterations are directly coupled with physiological responses (von Wirén and Bennett, 2016) and how fast they occur, suggesting that some specific pathways involved in Fe stress response are poorly known. In young maize seedlings subjected to nutritional deficiencies, Li et al. (2015) concluded that root hairs might sense the external lack of a specific nutrient and adjust their metabolism accordingly. In general, it has been reported that alterations in root morphology start before visible leaf chlorosis symptoms. In sugar beet, latent Fe deficiency induces subapical swelling with root hairs and the formation of transfer cells (Landsberg, 1995). In Fe-efficient potato genotypes (a strategy I species), root hairs and the formation of lateral roots were enhanced if the plants were grown under Fe deficiency conditions. At the physiological level, there was an increased expression of ferritin in the leaves and of an iron-regulated transporter (irt1) in the roots (Boamponsem et al., 2017). Kawahara and Kitamura (2015) reported that the swelling of root tips in Hyoscyamus albus L. (Solanaceae) subjected to Fe depletion was related to changes in both cell size and number, and to the development of root hairs. In our work, 3 days after Fe depletion (3 DAT), no chlorosis symptoms were developed in the aerial plant parts (Tab. 1). The chlorophyll concentrations in the leaves (young and mature) (Fig. 3) and several biomass parameters were not affected during this early stage of Fe stress (Tab. 3). However, root modifications began at this stage, which was supported by the high number of secondary roots in Fe-deficient plants (Fig. 5A). We may assume that an initial stress signal produced during root differentiation (at 3 DAT) was involved, and may subsequently trigger morphological and physiological response mechanisms to Fe deficiency. Therefore, in tomato plants, the period between 3 and 6 DAT seems to be critical to Fe stress response, and it is possible that an Fe-stress signal might be involved. Kobayashi and Nishizawa (2014) reviewed the nature of Festress signals and proposed several molecules as candidates: the iron itself, other metals, oxygen, the redox status, or haem and iron-sulphur clusters. Auxins play a significant role in the response of root morphology to Fe deficiency, by altering root architecture (Giehl et al., 2012; Hindt and Guerinot, 2012), but other compounds such as nicotianamine or nitric oxide (NO) may also be important in Fe long-distance transport and Fe homeostasis. In fact, a higher NO level in Fe-deficient roots enhanced Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC M.R. Jiménez, L. Casanova, T. Saavedra, F. Gama, M.P. Suárez, P.J. Correia, M. Pestana 231 Table 4. Pearson’s correlation coefficients (r) between the calculated values of total chlorophyll concentration in young leaves (dependent variable) and several plant parameters on different dates throughout the experiment. Iron treatments were analysed as one (n = 176). Only the significant (0.0001 < p < 0.05) correlations are shown. Negative slopes (inverse relations) are shown at the bottom DAT*rSignificance Plant height (mm) 14 0.87 **** Mature leaves – fresh weight (g) 14 0.83 **** Stem fresh weight (g) 14 0.79 **** Mature leaves – fresh weight (FW, g) 9 0.76 **** Roots – FCR activity (nmol Fe(II) min-1 g-1 FW) 14 0.75 **** Mature leaves – dry weight (g) 9 0.73 **** Mature leaves – chlorophyll (µmol m-2) 14 0.73 **** Mature leaves – dry weight (g) 14 0.72 **** Stem diameter (mm) 14 0.72 **** Total root volume (mL) 14 0.71 **** Number of leaves 14 0.69 **** Plant height (mm) 9 0.66 **** Young leaves – fresh weight (g) 14 0.66 **** Number of leaves 9 0.64 *** Roots – fresh weight (g) 14 0.61 *** Stem dry weight (g) 14 0.60 *** Stem fresh weight (g) 9 0.59 ** Mature leaves – fresh weight (g) 3 0.58 ** Young leaves – dry weight (g) 14 0.57 ** Young leaves – fresh weight (g) 9 0.54 ** Mature leaves – chlorophyll (µmol m-2) 9 0.53 ** Young leaves – dry weight (g) 9 0.51 ** Mature leaves – chlorophyll (µmol m-2) 3 0.49 * Roots – FCR activity (nmol Fe(II) min-1 g-1 FW) 9 0.49 ** Young leaves – fresh weight (g) 3 0.47 * Roots – dry weight (g) 3 0.43 * Stem diameter (mm) 9 0.43 * Total root volume (mL) 9 0.41 * Roots – fresh weight (g) 9 0.39 * Stem dry weight (g) 9 0.38 * Roots – dry weight (g) 9 -0.41 * Subapical swelling of roots at 0.5 mm 9 -0.54 ** Secondary roots in the first 2.0 cm from the root tip 9 -0.61 *** Roots – dry weight (g) 14 -0.62 *** Subapical swelling of roots at 1.0 mm 9 -0.66 **** Subapical swelling of roots at 1.5 mm 9 -0.72 **** Subapical swelling of roots at 2.0 mm 9 -0.72 **** Subapical swelling of roots at 0.5 mm 14 -0.74 **** Subapical swelling of roots at 1.0 mm 14 -0.78 **** Subapical swelling of roots at 1.5 mm 14 -0.79 **** Subapical swelling of roots at 2.0 mm 14 -0.80 **** *DAT: days after transplantation. Significance: * p < 0.05; ** p < 0.01; *** p < 0.001, and **** p < 0.0001 Bereitgestellt von Biblioteca de la Universidad de Sevilla | Heruntergeladen 18.09.19 11:08 UTC