An Introgression of Solanum habrochaites in the Rootstock Improves Stomatal Regulation and Leaf Area Development of Grafted Tomatoes under Drought and Low Root-Zone-Temperatures

Physiological traits improving drought and, since adaptation to cold and drought is to some extent regulated by the same genetic mechanisms, low root zone tolerance in tomatoes. The parental lines of an IL library and ILs carrying quantitative trait loci (QTL) alleles for cold tolerance introgressed from S. habrochaites were used as plant material. The recurrent parent (RP) was grafted onto the IL (IL/RP) and self-grafted (RP/RP). Grafted plants were grown


Introduction
Extremely low and high temperatures, prolonged drought and water logging, soil salinity, etc. are very common abiotic stresses responsible mainly for low harvest [1]. Tomato (S. lycopersicum L.) is a widely distributed vegetable susceptible to suboptimal temperatures [2]. In comparison to greenhouse tomatoes, open field tomatoes are directly connected with and adversely affected by abiotic factors. Drought and Temperature stress inhibit the productivity and limits the growing season and area [3]. Root hydraulic conductance of plant is substantially reduced by exposure to low temperatures. This severely decreases the conductivity of the critical membrane in roots and at the same time water viscosity increases [4]. Ultimately it reduces water absorption and may induce shoot water stress ('chilling55 drought'). As a result, tomato leaves quickly start to wilt and photosynthesis and transpiration decreases [5]. 56 Low temperature conditions and water deficit environments are independent phenomena but cold tolerant genotypes exhibit xerophytic adaptations [6] and synthesize the plant hormone ABA with higher concentration and delivery rate in xylem sap [7] to reduce the chilling effects. Cultivated and wild tomatoes responded differently to environmental stress [8]. The shoots of chilling susceptible tomato genotypes wilted under low-root zone temperature (around 5°C) while the same treatment did not affect S. habrochaites. In S. habrochaites, stomatal resistance increased as root temperatures decreased, whereas the stomata of S. lycopersicum remained open until the RZT reached 5°C [9]. A study analyzing the post-chilling shoot re-growth capacity of S. lycopersicum, S. pimpinellifolium, S. peruvianum, and S. habrochaites revealed that its wild relatives behaved superior to cultivated tomato [10]. Osmotic adjustment (OA) has been reported as an effective component of drought resistance in plants. It assists cell turgor maintenance at a given leaf water potential and delays wilting [11]. OA demands net increase in cellular osmolality through the accumulation of osmolytes [12]. It helps to maintain cell volume and leaf turgor and supports stomatal conductance and carbon assimilation under drought stress conditions [11,13]. Genetic variation among tomato species is important to develop stress tolerant lines. Wild tomato species are useful sources of genetic materials that can be introgressed into cultivated tomato for improving tolerance to chilling temperatures, drought and salinity [14,15]. Thirteen wild tomato species have been recognized as a source material to improve productivity and fruit quality of cultivated tomatoes [16,17]. Found a minimum of three QTLs affecting growth at low temperature in an interspecific S. lycopersicum 81 x S. habrochaites backcross population. Several IL libraries with wild Solanum species as donors were developed in the past. Ninety eight ILs with S. habrochaites as donor cover more than 85% of the donor genome [18]. IL-libraries are an effective genetic pool to identify QTLs and study their effects in contrasting environmental conditions. In the recent past, a major QTL controlling chilling tolerance was identified [19]. The goal of the present study was to analyze effects of a major QTL (shoot turgor maintainer, stm9), which is believed to confer cold tolerance [19], agronomic and physiological performance of grafted tomatoes with introgression lines as rootstocks. Tomato grafting is gaining popularity among commercial growers to improve productivity and quality [20,21], and to achieve tolerances against multiple abiotic stresses [22][23][24]. The study hypothesized that rootstocks with introgressions on QTL regions improving abiotic stress tolerance may improve crop productivity without inferring negative effects on agronomic traits since the above ground plant part does not include introgressions and its possible negative effects on yield and product quality.

Plant materials
Introgression lines (ILs) LA3957 that represent the genome of S. habrochaites (LA1777) in the background of S. lycopersicum cv. E-6203 (LA4024), recurrent parent (RP) from the same cross (LA4024), and the donor (D) S. habrochaites were used as plant materials. During the first experiment (Expt 1), all three genotypes (IL, RP, and D) and in second experiment (Expt 2), IL and RP were used. The IL which carries the chilling tolerance QTL allele (stm9) was used as rootstock. Seeds of all genotypes were obtained from the Institute of Plant Nutrition. Two 105 experiments were conducted from 14 July -17 August 2009 and 29 April -2 June 2010, 34 days at the Institute of Horticultural Production System, Leibniz University Hannover in a well-ventilated greenhouse under natural light condition.

Seedling preparation
Seedlings were prepared as per practices being carried out in the Vegetable System Modelling section and guidelines described by Black et al. [25]. n Expt 1, donor was sown eight days earlier than others due to the slow growth rate of seedlings. Scions were sown three days after sowing rootstocks to get equal stem diameters of seedlings. In both experiments, seedlings for rootstocks were transplanted individually to 450 ml plastic pots. Scion seedlings were thinned to one seedling and continued growing on the same tray. Grafting was done at fourth true leaf stage that was obtained approximately 17 days after sowing. The Japanese top grafting (tube grafting) method described by Oda et al. [26] was used with slight modifications. A horizontal 90° cut across stem axis was given instead of slanting cut. Finally, four different graft combinations in the Expt 1 and two in the Expt 2 were prepared as shown in (Table 1). Graft healing was done in healing tunnels under high RH at 20°C air temperature. After day 8 grafts were hardened in greenhouse at 20°C for seven days.

Experimental set up and stress treatment
A two factorial experimental set up was designed from two RZT and two levels of soil moisture. Well-watered condition and high RZT (25 ± 2°C) was the control. The same RZT was used for the drought condition. The low RZT (10 ± 2°C) was combined with well-watered condition (hereafter referred as 'cold treatment'). Grafted plants were completely randomized in climate chamber with 24/22°C day and night temperature and ventilation opened above 25°C. Soil temperature was maintained as described by Gosselin and Trudel [27] with modifications. In Expt 1, 0.5 litre capacity plastic pots (10 cm × 7.5 cm × 10 cm) without drainage hole were used while during Expt 2 plants 130 were grown in 1 litre pots (16.15 cm × 11.25 cm × 5.5 cm). Cold water (<8°C) from the cooling pipe circulated continuousl through double layered copper pipes in two containers in order to maintain low water bath temperature and thereby low soil temperature (10 ± 2°C) in the plastic pot. The water bath was placed on styrofoam and covered by the styrofoam to provide insulation for maintaining a constant water temperature. Four other containers were also covered by styrofoam to minimize evaporation. Soil and ambient air temperature was recorded daily using Technoterm 7300 (Testoterm, Lenzkirch, Germany). All plants were well-watered with Scotts Universol Orange water soluble fertilizer solution (500 g per 10 litre water). Once treatment started, plants in control and cold treatment were irrigated daily while plants subjected to drought were well-watered only during stress cycle break. An equal amount of water was applied to all plants of control and drought treatment. Drought stress was induced by withholding water until soil completely dried out. Length of stress cycle was affected by pot size used and weather condition. On an average, five-day long stress cycles were used in both experiments and plants were irrigated with an equal amount of water as shown in Table 2 by using pipettes fitted measuring cylinders.

Leaf stomata resistance and chlorophyll content
The terminal leaflet of fully expanded young leaf in comparable growth stages was chosen to measure stomata resistance on abaxial surface. The leaf blade was inserted carefully into the porometer (AP4, Delta-T Devices Ltd., Cambridge) head cuvette avoiding the leaf midrib being covered. Measurements were taken in the afternoon. Additionally leaf stomatal behavior in drought treatment was recorded 3 h after each stress cycle break and expressed as sm-1. Ten measurements were averaged for lower, middle, and upper leaves for the leaf chlorophyll content as 'SPAD index' using chlorophyll meter (SPAD-502 Plus, Konica Minolta Sensing Inc.).

Osmotic adjustment (OA)
OA was calculated based 155 on leaf relative water content (RWC) and osmotic potential (OP). RWC and OP were estimated on the youngest fully expanded leaves. Plants of the drought, cold and control treatment were re-watered in the evening before samples were taken. For determination of RWC, leaf disks (2.5 cm) were excised using a cork borer and immediately weighed to determine fresh weight (FW). Samples were placed into covered petri dishes filled with deionized  water and kept for 24 h in dim illumination at 20°C to reach full hydration. Individual leaf samples were surface dried with a paper towel and weighed immediately for the turgid weight (TW). Finally, samples were dried at 105°C to weight constant in order to obtain the dry weight (DW). Leaf RWC for cold (RWCc), well-watered (RWCw) and drought (RWCd) were calculated separately using the following formula:

TW -DW
For the leaf OP measurement, 0.7 cm leaf disks were detached carefully from the plants using a cork borer immediately wrapped in aluminum foil and placed in liquid nitrogen. Samples were stored at -20°C. OP was measured with pre-calibrated C-52 chambers (C-52 Chamber; Wescor Inc., Logan, Utah). OA was determined as the difference in measured osmotic potential (OP) between non-stressed and stressed leaves. Ludlow's full-turgor adjustment method was followed as described in Masinde [28] to calculate OA. In this method bound water is neglected and leaf OP at full turgor (OP100) of both stressed and non-stressed plants is given by:

Wilting score
Plants in the stressed were given wilting scores from 0 to 4; 0 for fully turgid plant, 1 for slightly wilted, 2 for moderately wilted, highly wilted scored 3, and 4 for flaccid plant. Scoring was done based on visual observations before each stress cycle break.

Green, non-green and total leaf area
Leaf area meter (model 3100, Li-COR, Lincoln) was used to obtain the total leaf area of individual plant. Freshly harvested leaves were individually scanned using a flatbed color image optical scanner

Dry mass production and partitioning, and tolerance index
Individual plant parts were divided into root, stem, and leaf consequently to get respective dry mass. Root shoot ratio (R: S) for individual plant was assessed as a ratio of root dry mass to above ground dry mass. Similarly, stress tolerance index (TI) was determined based on the method postulated by Foolad and Lin [29] as a ratio of total shoot dry matter produced in stress treatment to shoot dry mass in control and expressed as percentage. All the data obtained were presented as means and standard errors of the means. Where meaningful, data were subjected to analysis of variance (ANOVA), correlation analysis (r) using the R statistical package (Version 2.9.2, R Foundation for Statistical Computing, Vienna, Austria). For multiple comparisons of means Tukey 200 test was used. In the results and discussion sections, cold or cold treatment is frequently used for low RZT where reasonable.

Results
Results from comparison of means of measured parameters showed meaningful interrelation and interaction between factors. There was significant interaction in parameters like root dry matter (RDM), nongreen leaf area (NGLA), leaf chlorophyll index and stomatal resistance (RS). Graft x treatment interactions were not significant in parameters like leaf dry matter (LDM), total dry matter (TDM), total leaf area (TLA), and green leaf area (GLA) ( Table 3) and overall graft and treatment means were compared and results interpreted accordingly. Leaf area parameters and plant parts dry matter portioning were affected by low RZT and drought.

Leaf area
In both experiments, the IL/RP produced significantly higher TLA (17.33%) and GLA (14.75%) than RP/RP (Table 4). Mean NGLA values between graft combinations (GCs) were not significant under the control treatment in Expt 1 and 2. In contrast to this, all four graft combinations were significantly different among each other in the cold treatment in Expt 1. RP/RP resulted to significantly higher NGLA compared to IL/RP under cold (36.8%) and drought (32.35%) treatment. The D/RP has produced the least NGLA (23.68 ± 0.573 cm -2 ) under cold, however fairly higher (22.3%) than IL/RP under drought in Expt 1 (Table 5). Strong positive correlation was found among GLA, TLA, LDM, RDM, and TDM ( Table 6).

Leaf chlorophyll content
Significant genotype x environment interaction on leaf chlorophyll content (LCC) of upper, middle, and lower canopy leaves was observed. Comparison of upper leaf LCC between IL/RP and RP/ RP in Expt 1 and Expt 2 was not significant under control and cold but IL/RP resulted significantly higher LCC (10.65%) under drought condition. Similar trend was observed 224 in middle leaf LCC in both experiments however, LCC mean difference between IL/RP and RP/RP found significant under both stress environments. IL/RP produced 6% under cold and 7.3% higher LCC under drought than RP/RP. Data on lower canopy LCC ranges from 27.6 to 42.2 and revealed the similar result pattern that was observed in case of middle and upper leaf LCC. Leaf chlorophyll content produced by IL/RP significantly higher than RP/RP under cold (16.5%) and drought (20.5%) ( Table 5).

Dry matter produced and partitioning
Accumulated dry matter in plant parts significantly varied with different growing conditions. Treatment mean comparisons for LDM, RDM, and TDM showed that grafts produced higher dry mass under control. Drought LDM mean was significantly higher than cold LDM in both experiments. However means for RDM and TDM under cold and drought stress treatment were statistically not different. Significant genotype x treatment interaction was noted in RDM in Expt 1 but not in Expt 2 (Table 3). Averaged across treatments, in both experiments IL/RP produced significantly higher LDM than RP/RP. It is 26 % higher in Expt 1, 13.75 % in Expt2 (Table 4). Significant TDM differences were observed among treatments and graft combinations (GCs) in both experiments. In Expt 1, IL/RP produced significantly higher TDM (11.703 ± 0.301) than those of D/RP (    Similar result was observed in the drought where IL/RP produced significantly higher RDM (1.145 ± 0.128) than that of D/RP (0.637 ± 0.079). Other comparisons were not significant. In Expt 2, averaged 249 across treatments, IL/RP produced 44.5% higher RDM than RP/ RP (Table 4). Strong correlation was observed between TLA and TDM (r=0.935, Df=48, level of significance *** P<0.001) ( Table 6). There were no marked differences in averaged root shoot ratio (R: S) data from Expt 1 although IL/RP showed slightly higher ratio than D/RP and RP/RP. In Expt 2, IL/RP produced significantly higher R: S than RP/RP which is 33.3% higher. Similarly, averaged across treatments, mean R: S value for the cold treatment was fairly higher than control in Expt 2 (Table 7).

Stomata conductance
Stomatal behavior of treated plants were observed as a leaf stomatal resistance (RS) and expressed as sm -1 . Test statistics on SR showed highly significant genotype x treatment interaction (P ≤ 0.05) ( Table  3). Result clearly showed that IL/RP graft combination highly resisted to stomata opening compared to RP/RP under environmental stress condition. No difference between graft combinations was observed under control in both experiments. However, there was marked differences in SR under drought and cold treatments. The IL/RP showed 98% and 113.5% higher RS than RP/RP in cold and drought treatment respectively (Figure 1). Similar result observed between D/ RP and RP/RP in Expt 1, where D/RP was 109.2% more resisted than RP/RP. Data on stomatal resistance obtained 3 hours after drought stress break showed contrasting result than those incurred from regular measurement. During stress recovery process in both experiments, significantly faster recovery in stomatal conductance was noticed. In Expt 1, both D/RP (1624.5 ± 42.7) and IL/RP (1713.1 ± 50) significantly lowered down the RS than RP/RP (1901.3 ± 32.1). Similar to the result in Expt 1, in Expt 2 also IL/RP showed significantly lower RS (1657 ± 36.2) compared to RP/RP (1752.2 ± 50.9) (P ≤ 0.05) (Figure 2).

Osmotic adjustment
Different statistics on osmotic adjustment (OA) were found among treatments and GCs. In Expt 1, mean OA (MPa) in drought treatment was significantly higher than cold. The D/RP graft combination 274 showed significantly higher OA compared to RP/RP. No significant difference was found among other GCs. In Expt 2, IL/RP tended to be higher in OA than RP/RP, and mean OA in drought stress was numerically higher than cold. However, OAs among treatments and graft combinations were not statistically different (Table 8).

Wilting scores
Tomato graft combinations responded differentially in wilting under the drought. The RP/RP plants responded strongly to water stress with the highest score. D/RP was less affected resulting the lowest score. Wilting scores produced by all four graft combinations were significantly different among each other. Similar result observed in Expt 2 where RP/RP affected by stress and produced significantly higher score than IL/RP (Figure 3).

Tolerance index
A mean TI (%) of IL/RP was significantly higher than that of RP/ RP (P ≤ 0.05) in both experiments ( Table 9). The IL/RP showed 42.33% higher TI in Expt 1 and 18.58% in Expt 2 than RP/RP. No statistical difference was found between averaged TI of cold and drought. A highly significant correlation was observed between TI and total dry matter produced under stressed environments (r=0.66 in Expt 1 and 0.96 in Expt 2, n=32, level of significance ***P<0.001).

Discussion
In the present study, an attempt has been made to explore dynamics of cold and drought stress tolerance in tomato introgression lines. It studied tomato ILs together with its donor and recurrent parent and examined some major physiological traits involved in cold and drought tolerance. The main focus of this study was to compare the two graft combinations IL/RP and RP/RP under different environmental conditions. Results clearly showed the differential response of tomato genotypes to low RZT (cold) and drought. Observed variation in agronomic traits can be due to genetic 298 or morphological or environmental factors [8,30,31] or combination of them. Abiotic stress tolerance is a genetically controlled phenomena based on additive QTL-effects [29]. The present study elucidated higher green leaf area and lower non-green leaf area for IL/RP compared to self-grafted RP in stress conditions (Tables 4 and 5). A similar pattern was also observed for the leaf chlorophyll content. This, together with wilting symptoms recorded on IL/RP (Figure 3), indicates a higher tolerance of IL/RP to cold and drought compared to RP/RP. In agreement to the results, higher green area, chlorophyll content in leaf and photosynthesis rate were recorded for S. peruvianum, a chilling tolerant wild tomato, compared to cultivated tomato cultivar under chilling stress [32]. Strong variation was noticed on leaf chlorophyll content. Significantly higher chlorophyll index in lower and middle leaves were observed in IL/RP compared to RP/RP under the cold and drought treatment ( Table 5) and upper leaf chlorophyll index was only different in water stress condition. This indicates that leaf chlorophyll content is also a physiological parameter affected by abiotic stress and it varies among genotypes. Compared to drought tolerant wild tomato (S. pennellii), significant yellowing of lower leaves and low chlorophyll contents were also reported by Torrecillas et al. [33] in cultivated tomato during 7 days long water stress condition. The presented data on chlorophyll     [34] who reported that chlorophyll content was significantly higher in a drought tolerant barley genotype compared to genotypes sensitive to water stress. The data supports the hypothesis that stress tolerant genotypes slow down the wilting processes and maintain green leaf area and growth. Significant effect of suboptimal growing conditions was observed in root, leaf and stem dry matter deposition (Table 4). Averaged across the treatments, total leaf area in the cold treatment was found to be lower compared to the drought and control condition. This may be 323 due to continuous low RZT stress in the cold treatment whereas plants under drought were re-watered during stress cycle break that could have led to better leaf expansion. Though leaf expansion rate was not assessed in the current study, observed reduced leaf area found in soybean showed that severe stress reduced leaf size due to poor leaf expansion rates in cold susceptible soybean genotypes [35]. Current result on dry matter is consistent to the result by Balibrea et al. [36] working on tomato who reported that leaf area and total dry matter were significantly affected by the salinity in salt sensitive genotype. A similar result was also observed by Katerji et al. [37] in tomato. Leaf area is important because it has direct impact on photosynthesis. This can be due to the strong correlation between leaf area and carbon assimilation rate, which is directly related to the plant growth and total biomass production [38]. Strong correlation between total leaf area and total dry mass was observed in recent study (Table 6). Larger leaf area and higher dry matter produced by plant indicates that IL/RP performed better under stress condition than RP/RP. Supporting the current findings, a study has confirmed the comparable increment in net photosynthesis in cultivated tomato grafted onto S. Mammosum in contrast to selfgrafted tomatoes under water stress [39]. Further support comes from a study that revealed the greater capacity of S. habrochaites for CO 2 uptake compared to common tomato as before and after chilling exposure [36,40,41] found significantly higher net photosynthesis rate in salt tolerant tomatoes with positive correlation between photosynthesis and plant growth. Higher total leaf area of IL/RP indicates the higher relative growth rate of IL/RP in comparison to RP/ RP under low RZT. This result is consistent with the work done by van der Ploeg et al. [42] who compared ungrafted S. pennellii, S. habrochaites, and common tomato cultivar in low temperature. Markedly reduced relative growth rate in the commercial tomato cultivar was mainly attributed to decreased leaf area. 348 The present study, however unable to compare D/RP graft performance in the second experiment due to lack of seed but the results from the Expt 1 showed significant difference in total leaf area between IL/RP and D/RP under cold and drought stress. Significant variation between graft combinations in leaf area and leaf dry mass was also pronounced in the present study. This is in agreement with the result from the study on cultivated and wild tomatoes (S. habrochaites and S. peruvianum) where interspecific comparison showed significant variations among the measured traits [43] Similar results were found in tomato grafted onto rootstocks of S. habrochaites in low RZT [24] Differential response of graft combinations   to root shoot ratio (R: S) under stress was observed in this study ( Table  7). The IL/RP produced significantly higher R: S compared to RP/RP in the Expt 2 while tended to be higher in the Expt 1. The finding is also resembled with findings from Torrecillas [33] working on tomato. It has been reported lower R: S in cultivated tomato compared to S. pennellii. In hot pepper, significantly higher R: S was observed in the drought stressed plants compared to the well-watered [44] it can be concluded that ILs have high capacity to adjust their R: S to stress environment in comparison with the RP. Increasing R: S at 10°C RZT may adjust the root system to overcome the lower water absorption due to decreased root hydraulic conductivity and increased water viscosity [9,45]. Significant interaction between treatment and graft combinations in root dry mass indicates that the effect of the growing condition depends on the genotype used. More interestingly, IL/RP was able to produce higher root dry matter than D/RP and RP/RP under cold and drought stress. This result indicates that IL as a rootstocks can develop underground plant part better than donor rootstocks or the RP. According to the findings of Venema et al. [24] common tomato grafted onto S. habrochaites rootstock produced higher leaf and root dry matter in low RZT and root to shoot ratio (373 R: S) was also higher. Although a detailed study is required for comparative root morphological analysis observed higher root dry matter and larger R: S indicates the strong variation in root growth rate between the rootstocks used. Results from the current study elucidated higher genotypic variation in stomatal closure. Higher stomatal resistance was observed in IL/RP under both stress environment. In contrast to this, the same graft combination showed higher stomatal conductance few hours after drought stress cycle break. This indicates that drought tolerance of IL/RP is due to more efficient stomatal control. In agreement with this result, higher stomatal resistances were also reported for S. pennellii under drought stress [33], and for S. habrochaites in low RZT [9]. A similar result was found in S. cheesmaniae, S. chmielewskii, S. lycopersicum var. cerasiforme, S. neorickii and S. pimpinellifolium [46] where significantly higher stomatal resistance was observed under drought condition compared to the control. Apparently current result contradicts the comparatively larger biomass accumulation in IL/RP while persisted higher stomatal resistance. The reason is not so clear but some contextual findings in past studies may support the outcomes. Vallejos and Pearcy [47] demonstrated that S. habrochaites and its hybrid (developed by crossing with S. lycopersicum) showed faster acclimatization at low temperature by increased photosynthetic rates. Choluj et al. [48] showed a positive linear relationship between the net gas exchange and stomatal conductance in chilling tolerant tomato cultivars under short-term chilling condition. They found no significant effect of stomatal resistance in net CO 2 assimilation when tolerant tomato genotype shortly exposed to chilling temperature (2°C). Similar study with a chilling tolerant maize cultivar showed that net assimilation rate was comparatively higher than that of sensitive one and it reached control values after stress release [49]. Another study on tomato 398 grafted onto S. mammosum showed the comparable increment in net photosynthesis and leaf conductance in contrast to self-grafted tomato cultivars in water stress condition [39]. More recently, Campos et al. [50] in tomato reported that carbon assimilation rate was not affected by partial drought compared to control, however, higher stomatal resistance and lower transpiration were observed. Stomatal resistance of IL/RP after stress cycle break was significantly lower than that of RP/ RP ( Figure 2). Such recovery in stomatal regulation in IL/RP may lead to vegetative growth recovery which can be the reason for higher green leaf area and total leaf area, and so as higher carbon fixation. A study on wild tomatoes revealed a rapid recovery in stomatal conductance and net assimilation after breaking the water stress [46,51] Easlon, Richards, Anyia and Herzog observed the same pattern of recovery in cowpea. Water stressed plants showed higher dry matter gain than unstressed plants when re-watered after a week-long stress. Compensatory growth was evidenced during the recovery process. Sharp et al. [52] showed that tolerant tomato genotypes recovered shoot growth due to endogenous ABA accumulation. Findings of Sharp et al. support the hypothesis that higher ABA concentration in tomato leaf caused early stomata closure, and post stress ABA involvement in leaf expansion and shoot growth recovery [53,54]. Current result is in line with the results from cowpea and tomatoes and it supports the hypothesis that higher stomatal resistance during stress and low stomatal resistance during recovery result into higher biomass production in tolerant tomato genotypes. Results showed that IL/RP demonstrated higher stomatal resistance and higher biomass deposition under continuous cold treatment compared to self-grafted RP/RP plants. This could be due the genotypes used as rootstocks. ILs rootstocks carrying QTL allele, stm9, for cold tolerance may have a positive effect in stomatal behavior resulting shoot turgor and higher biomass. Although, the response of genotypes after cold stress break was not estimated, but based on the drought recovery observations 423 similar phenotypic variation among graft combinations can be presumed. Higher total leaf area, green leaf area, leaf dry matter in drought treatment compared to the cold clearly reflects the stress break affect the overall plant growth and development. Past studies uncovered the faster biosynthesis of ABA in cold tolerant maize [55] and tomato genotypes [7]. Faster ABA biosynthesis was responsible for early stomata closure. As reviewed by Blum [56] higher biomass production is associated with faster poststress recovery with reducing stomatal resistance that allows greater carbon fixation and transpiration. This recovery capacity appears to be important for the final yield. Osmotic adjustment value obtained for IL/RP was not large enough to show a difference from RP/RP but it produced higher total dry matter ( Table 8). As reported by Blum [57] plants may not respond to osmotic adjustment under rapidly imposed stress environment because it is a slow process and takes more time to the adjustment depending upon the genotype. However, this result is in line with the finding of Bloom et al. [9] who reported the non-significant response of grafted tomato on shoot turgor maintenance. This result supports the hypothesis that the osmotic adjustment is part of whole to obtain stress tolerance. It may contribute to but not a major contributor for stress tolerance in plants under stress environments [58]. The nonsignificance correlation between osmotic adjustment and total dry matter from this study is consistent with the result observed by Katerji et al. [37] in tomato where non-significant correlation was found between osmotic adjustment and total dry mass under salt stress. Results showed significant wilting responses of graft combinations to drought. Significantly low wilting scores of IL/RP is in agreement with the findings from Bloom et al. [9] working in tomato. Chilling sensitive genotype resulted into higher wilting scores compared to the tolerant one when exposed to 4°C for 2 h. Present work, however, did not study the wilting response to cold but similar genotypic response 448 can be estimated based on the previous findings and current observations. Present study elucidated that IL/RP results in higher tolerance index ( Table 9). The tolerance index was highly correlated with total biomass produced. This is consistent with the findings of Foolad and Lin [29] in tomatoes where such index of the filial and backcross progenies of cold tolerant parents was significantly higher than those of a cold-sensitive tomatoes. Further total dry mass and tolerance index was highly correlated. Significantly higher tolerance index of IL/RP than RP/RP indicates the superior performance of the IL/RP due to an inherent abiotic stress tolerance of ILs. Rao et al. [41] working on tomato  [59] came to the similar conclusion and mentioned that salt tolerance is as a result of additive genetic control. This supports the statement that tolerance index is one of the important tools to compare the genotype based on their phenotypic performances. This study succeeded to graft recurrent parent onto the S. habrochaites rootstocks (D/RP) under normal greenhouse conditions with higher survival rate. Earlier such type of interspecific grafting was reported as incompatible [9]. Data on higher performance of IL rootstocks under suboptimal growing condition are highly consistent with previously published data and suggest that ILs can replace rootstocks in the conventional grafting practices. Under adverse growth conditions total dry matter of cultivated tomato grafted with tolerant rootstocks was considerably higher than self-grafted plants [21,24,25]. The basis for argument can be more genetic, for instance the expression of favorable alleles introgressed from the wild relative S. habrochaites. In their work on tomatoes [14,18,19,60]

Conclusion
This study can describe logically the agronomical parameters and physiological basis of low RZT and drought tolerance in tomato. Low RZT and drought hampered plant function and substantially reduced carbon assimilation. Grafted plants onto ILs rootstocks performed better than self-grafted RP in terms of leaf area, dry matter production, and showed better recovery ability after drought release. The parameters studied herein suggest that IL/RP efficiently controlled stomata opening and maintained growth under stress and proved comparatively higher tolerance to low RZT and drought. When tomato is grafted onto IL LA3957, the stomatal resistance increases in response to cold and drought stress so that leaf turgor (and therefore growth) can be stabilized. This in contrast to self-grafted tomato plants which show symptoms of wilting and senescence. The green and total leaf area, stomatal resistance, root shoot ratio, and tolerance index can be considered as potential physiological markers for cold and drought tolerance study in tomato breeding. ILs appeared to be a valuable gene pool for tomato breeding to improve low temperature and drought tolerant'energy-efficient' tomato cultivars.