The Influence of the Partitioning of Sugars, Starch, and Free Proline in Various Organs of Cyclamen graecum on the Biology of the Species and Its Resistance to Abiotic Stressors

The geophyte Cyclamen graecum is native to the eastern Mediterranean. Its beautiful flowers with upswept pink petals appear during early autumn, after the summer drought period and before leaf expansion in late autumn. The floral and leaf development alternates with their cessation in early winter and late spring, respectively. Ecophysiological parameters and processes underlining the life-cycle of C. graecum have not previously been published. Seasonal fluctuations of sugars, starch, and free proline have been investigated in tubers, leaves, pedicels, and petals, as well as petal and leaf water status. At the whole plant level, the seasonal co-existence of leaves and flowers is marked by an elevated soluble sugar content, which was gradually reduced as the above-ground plant parts shed. The sugar content of petals and pedicels was lower than that of leaves and tubers. Leaf starch content increased from late autumn to spring and was comparable to that of tubers. The starch content in petals and pedicels was substantially lower than that of tubers and leaves. In tubers, monthly proline accumulation was sustained at relatively constant values. Although the partitioning of proline in various organs did not show a considerable seasonal variation, resulting in an unchanged profile of the trends between tubers, leaves, and flowers, the seasonal differences in proline accumulation were remarkable at the whole plant level. The pronounced petal proline content during the flowering period seems to be associated with the maintenance of floral turgor. Leaf proline content increased with the advance of the growth season. The values of leaf relative water content were sustained fairly constant before the senescence stage, but lower than the typical values of turgid and transpiring leaves. Relationships of the studied parameters with rainfall indicate the responsiveness of C. graecum to water availability in its habitat in the Mediterranean ecosystem.


Introduction
The geophytes exhibit a life-cycle associated with temporal separation of the vegetative phase from the flowering phase and possess perennial tubers, which support their annual growth [1][2][3]. Cyclamen L. (Primulaceae) is commercially important and a very popular horticultural genus native to the area around the Mediterranean Basin [4][5][6]. Wild cyclamens are perennial geophytes of woods and rocky areas. Cyclamen was mentioned as kyklaminos (κυκλάµινoς) in Theophrastus' writings (4th century BC) [2,7]. The Cyclamen Society [8] recognizes 20 Cyclamen species. The cultivated cyclamens are usually hybrids of the spring flowering species Cyclamen persicum. September to leaf senescence in April) and the dormant phase spanning the pr drought period (from May to August) in the eastern Mediterranean, w aboveground plant parts are not visible. Concerning the active phenological st flowers splay open in September (Figures 1 and 2) before leaf emergence in No ( Figure 2). The seasonal floral and leaf development of C. graecum in early and late ( Figure 2) respectively alternates with cessation of flowers and leaves in winter an summer, respectively. There is a marked variation in the length of the period of fl and leafing that affects the capacity of this species for resource acquisition.  Iconographic presentation of the annual cycle and the phenological stages of C (using illustrations of flowers ( ), leaves ( ) and tubers ( )), i.e., the active phase ind the ivory area that includes flower initiation and longevity (September-December), emergence, development, longevity, and senescence (November-April), and the dorma indicated by the gray area that includes only the subterranean tubers, because above-groun is not visible.

Sugars
Tubers accumulated large quantities of soluble sugars throughout the year (F A gradual reduction of stored sugars in the tubers was detected in October, du flowering stage, and continued during November and December, when flow leaves co-existed. Sugar content of petals and pedicels was lower than that of lea tubers, reaching maxima in October. Strong monthly fluctuation of soluble s leaves was detected from November to April, with the maximum values being a by mature leaves of December. The considerable sugar content, which was estim tubers, declined during the coexistence of floral and leaf stage in Novem December. At the whole plant level, the co-existence of leaves and flowers ma   Iconographic presentation of the annual cycle and the phenological stages of C. graecum (using illustrations of flowers ( ), leaves ( ) and tubers ( )), i.e., the active phase indicated by the ivory area that includes flower initiation and longevity (September-December), and leaf emergence, development, longevity, and senescence (November-April), and the dormant phase indicated by the gray area that includes only the subterranean tubers, because above-ground growth is not visible.

Sugars
Tubers accumulated large quantities of soluble sugars throughout the year (Figure 3). A gradual reduction of stored sugars in the tubers was detected in October, during the flowering stage, and continued during November and December, when flowers and leaves co-existed. Sugar content of petals and pedicels was lower than that of leaves and tubers, reaching maxima in October. Strong monthly fluctuation of soluble sugars in leaves was detected from November to April, with the maximum values being achieved by mature leaves of December. The considerable sugar content, which was estimated in tubers, declined during the coexistence of floral and leaf stage in November and December. At the whole plant level, the co-existence of leaves and flowers marked the highest sugar content, which was gradually reduced as the above-ground plant parts shed, eventually entering the dormant phase. Monthly values of petal sugar content were   (Figures 1 and 2) before leaf emergence in November ( Figure 2). The seasonal floral and leaf development of C. graecum in early and late autumn ( Figure 2) respectively alternates with cessation of flowers and leaves in winter and before summer, respectively. There is a marked variation in the length of the period of flowering and leafing that affects the capacity of this species for resource acquisition.  Iconographic presentation of the annual cycle and the phenological stages of C. graecum (using illustrations of flowers ( ), leaves ( ) and tubers ( )), i.e., the active phase indicated by the ivory area that includes flower initiation and longevity (September-December), and leaf emergence, development, longevity, and senescence (November-April), and the dormant phase indicated by the gray area that includes only the subterranean tubers, because above-ground growth is not visible.

Sugars
Tubers accumulated large quantities of soluble sugars throughout the year (Figure 3). A gradual reduction of stored sugars in the tubers was detected in October, during the flowering stage, and continued during November and December, when flowers and leaves co-existed. Sugar content of petals and pedicels was lower than that of leaves and tubers, reaching maxima in October. Strong monthly fluctuation of soluble sugars in leaves was detected from November to April, with the maximum values being achieved by mature leaves of December. The considerable sugar content, which was estimated in tubers, declined during the coexistence of floral and leaf stage in November and December. At the whole plant level, the co-existence of leaves and flowers marked the highest sugar content, which was gradually reduced as the above-ground plant parts shed, eventually entering the dormant phase. Monthly values of petal sugar content were   Iconographic presentation of the annual cycle and the phenological stages of C. graecum (using illustrations of flowers ( ), leaves ( ) and tubers ( )), i.e., the active phase indicated by the ivory area that includes flower initiation and longevity (September-December), and leaf emergence, development, longevity, and senescence (November-April), and the dormant phase indicated by the gray area that includes only the subterranean tubers, because above-ground growth is not visible.

Sugars
Tubers accumulated large quantities of soluble sugars throughout the year (Figure 3). A gradual reduction of stored sugars in the tubers was detected in October, during the flowering stage, and continued during November and December, when flowers and leaves co-existed. Sugar content of petals and pedicels was lower than that of leaves and tubers, reaching maxima in October. Strong monthly fluctuation of soluble sugars in leaves was detected from November to April, with the maximum values being achieved by mature leaves of December. The considerable sugar content, which was estimated in tubers, declined during the coexistence of floral and leaf stage in November and December. At the whole plant level, the co-existence of leaves and flowers marked the highest sugar content, which was gradually reduced as the above-ground plant parts shed, eventually entering the dormant phase. Monthly values of petal sugar content were   Iconographic presentation of the annual cycle and the phenological stages of C. graecum (using illustrations of flowers ( ), leaves ( ) and tubers ( )), i.e., the active phase indicated by the ivory area that includes flower initiation and longevity (September-December), and leaf emergence, development, longevity, and senescence (November-April), and the dormant phase indicated by the gray area that includes only the subterranean tubers, because above-ground growth is not visible.

Sugars
Tubers accumulated large quantities of soluble sugars throughout the year ( Figure 3). A gradual reduction of stored sugars in the tubers was detected in October, during the flowering stage, and continued during November and December, when flowers and leaves co-existed. Sugar content of petals and pedicels was lower than that of leaves and tubers, reaching maxima in October. Strong monthly fluctuation of soluble sugars in leaves was detected from November to April, with the maximum values being achieved by mature leaves of December. The considerable sugar content, which was estimated in tubers, declined during the coexistence of floral and leaf stage in November and December. At the whole plant level, the co-existence of leaves and flowers marked the highest sugar content, which was gradually reduced as the above-ground plant parts shed, eventually entering the dormant phase. Monthly values of petal sugar content were )), i.e., the active phase indicated by the ivory area that includes flower initiation and longevity (September-December), and leaf emergence, development, longevity, and senescence (November-April), and the dormant phase indicated by the gray area that includes only the subterranean tubers, because above-ground growth is not visible.

Sugars
Tubers accumulated large quantities of soluble sugars throughout the year ( Figure 3). A gradual reduction of stored sugars in the tubers was detected in October, during the flowering stage, and continued during November and December, when flowers and leaves co-existed. Sugar content of petals and pedicels was lower than that of leaves and tubers, reaching maxima in October. Strong monthly fluctuation of soluble sugars in leaves was detected from November to April, with the maximum values being achieved by mature leaves of December. The considerable sugar content, which was estimated in tubers, declined during the coexistence of floral and leaf stage in November and December. At the whole plant level, the co-existence of leaves and flowers marked the highest sugar content, which was gradually reduced as the above-ground plant parts shed, eventually entering the dormant phase. Monthly values of petal sugar content were positively related with those of tubers (y = 0.523x − 3.882, R 2 = 0.889, p < 0.05) and pedicels (y = 1.227x − 30.461, Plants 2022, 11, 1254 4 of 13 R 2 = 0.609, p < 0.05), while leaf sugar content was negatively related with that of tubers (y = −0.494x + 337.030, R 2 = 0.591). In addition, the seasonal rainfall was negatively correlated with the sugar content of petals (y = −0.213x + 87.849, R 2 = 0.619, p < 0.05) and positively correlated with the sugar content of leaves (y = 0.098x + 17.322, R 2 = 0.709, p < 0.05).

Starch
The highest starch content in tubers of C. graecum was observed in April (256 mg g −1 ) when the climatic conditions were favorable for photosynthesis in the Mediterranean ecosystems, and before the cessation of foliar growth of C. graecum. Thereafter, from May to October, starch content declined ( Figure 4). The lowest values of starch content in tubers (80 mg g −1 ) were measured from June to October; actually, this period coincides the threemonth summer drought (June to August), the cessation of foliar growth, and the early stage of flower formation in September, before the development of new expanding leaves in November (Figure 2). Intermediate values of starch content were detected in tubers from November to January during the development of new leaves. The values of starch content in leaves increased from November to April and were comparable to those of the tubers ( Figure 4); in fact, seasonal variation of leaf starch content was positively related with that of tubers (y = 1.027x + 13.422, R² = 0.784, p < 0.05). The starch content in petals and pedicels was substantially lower than that of tubers and leaves during the flowering stage (from September to December) (

Starch
The highest starch content in tubers of C. graecum was observed in April (256 mg g −1 ) when the climatic conditions were favorable for photosynthesis in the Mediterranean ecosystems, and before the cessation of foliar growth of C. graecum. Thereafter, from May to October, starch content declined ( Figure 4). The lowest values of starch content in tubers (80 mg g −1 ) were measured from June to October; actually, this period coincides the three-month summer drought (June to August), the cessation of foliar growth, and the early stage of flower formation in September, before the development of new expanding leaves in November (Figure 2). Intermediate values of starch content were detected in tubers from November to January during the development of new leaves. The values of starch content in leaves increased from November to April and were comparable to those of the tubers ( Figure 4); in fact, seasonal variation of leaf starch content was positively related with that of tubers (y = 1.027x + 13.422, R 2 = 0.784, p < 0.05). The starch content in petals and pedicels was substantially lower than that of tubers and leaves during the flowering stage (from September to December) (Figure 2). The relatively elevated values of starch content in petals in September and October decreased in November and December (Figure 4), coinciding with elevated starch content in leaves (approximately from 100 to 140 mg g −1 d.w.). Negative relationships were detected between petal starch content with the corresponding tuber starch content (y = −0.632x + 125.930, R 2 = 0.892, p < 0.05) and the precipitation in the study site (y = −1.146x + 117.010, R 2 = 0.839, p < 0.05).

Proline
The partitioning of free proline in tubers, leaves, pedicels, and petals are presented in Figure 5. The tubers sustained an almost stable free proline content throughout the year, with a slight but statistically significant increase during the cold months (November to March). The pronounced free proline accumulation in petals was evident during the flowering stage showing a substantial enhancement during October and November, the period of full blossom. The pedicels contained a quantity of proline at a comparative level with that of the tubers. The proline content found in leaves during the first two months of their appearance is comparable with that of tubers, but it significantly increased during the next four months of the leaf-stage for this species. Accordingly, the partitioning of proline in the various plant parts did not show a considerable seasonal variation resulting in an unchanged profile of the trends between tubers, leaves, and flowers. Nevertheless, seasonal differences in proline accumulation were obvious at the whole plant level, with the contribution of the proline-rich petals being remarkable.

Proline
The partitioning of free proline in tubers, leaves, pedicels, and petals are presented in Figure 5. The tubers sustained an almost stable free proline content throughout the year, with a slight but statistically significant increase during the cold months (November to March). The pronounced free proline accumulation in petals was evident during the flowering stage showing a substantial enhancement during October and November, the period of full blossom. The pedicels contained a quantity of proline at a comparative level with that of the tubers. The proline content found in leaves during the first two months of their appearance is comparable with that of tubers, but it significantly increased during the next four months of the leaf-stage for this species. Accordingly, the partitioning of proline in the various plant parts did not show a considerable seasonal variation resulting in an unchanged profile of the trends between tubers, leaves, and flowers. Nevertheless, seasonal differences in proline accumulation were obvious at the whole plant level, with the contribution of the proline-rich petals being remarkable. five replicates ± standard error; Standard Errors smaller than the line thickness of the columns are not shown. Significant differences (p < 0.05) of mean values are marked using lowercase letters.
The relative water content (RWC) of leaves was sustained fairly constant until March and declined in April (Table 2). Additionally, a positive relationship was detected between RWC and rainfall (y = 0.2768x + 63.088, R 2 = 0.835, p < 0.05).

Discussion
The seasonal accumulation of starch and soluble sugars in the tubers of C. graecum confirms to their role in storing photoassimilates and providing a supply of energy to drive new growth [17,25]. The distribution between soluble carbohydrates and starch differed between leaves and tubers. The partitioning of starch to tubers was reasonably similar to that of leaves and a positive linear relationship was detected between tubers and leaves (y = 1.027x + 13.422, R 2 = 0.784, p < 0.05); starch partitioning may be linked to source-sink relationships; the photosynthetically active leaves (the source) provide assimilated carbon (available for transport) to a storage organ (sink), which will utilize it to support metabolic requirements. Furthermore, the elevated values of starch from February to April in both tubers and leaves coincide with the leaf photosynthetic efficiency, and the mild winter temperatures in the Mediterranean area that favor photosynthetic rates. It seems likely that in C. graecum, starch may represent a commitment of resources that are acquired by the above-ground tissues simultaneously with the growth of those drawn from stored reserves. This finding is in contrast to data published elsewhere for the summer flowering geophyte Pancratium maritimum, where starch was mainly stored in underground bulbs [26].
At the phenological stage of flowering, when the ambient temperatures begin to fall, the concentration of soluble sugars in the tubers rapidly decreased to support the metabolically demanding reproductive growth with carbon source and energy [27,28]; this is also indicated by the positive linear relationship between sugar content between tubers and petals (y = 0.523x − 3.882, R 2 = 0.881, p < 0.05). Floral growth during the early autumn takes precedence over allocation. A further decrease of soluble sugars in tubers at the period of leaf emergence indicates a translocation of stored sugars to sustain leaf development and floral exhibition, when winter lies ahead, via a transition from sink to source. The leaf sugar content during winter and spring denotes an active photosynthetic machinery for this species grown under ambient, environmental conditions, coinciding with the values of leaf RWC before wilting; leaf RWC may also be considered as a measure of the relative cellular volume, affecting interactions among macromolecules. Usually, levels of RWC below 70% imply a water potential at the order of −1.5 MPa or less, and this would cause changes in the metabolism with ceasing of photosynthesis [29], concomitantly with leaf senescence in April. Leaf sugar content may also be associated with the argument that leaves of cyclamen species are a static export pool of sucrose, and the sugar transport is probably linked to a time lag in the export of newly fixed carbon from leaves and low velocity of phloem transport [30]. Concerning the sugar partitioning, some geophytes seem to follow a pattern of relatively higher sugar concentration in the subterranean organs compared to leaves and in some cases, with flowers [31]. In petals, the reduced osmotic potential was significantly related with increased soluble sugar content (y = −0.0034x − 0.1663, R 2 = 0.834, p < 0.05), presumably contributing to turgor maintenance, expansion and water status of these tissues [32][33][34]. Actually, anthesis appears to be due to a pulsed increase in the concentration of soluble sugars [35][36][37][38]. A relationship linked to transfer of sugars between leaves and petals, which might be interesting, was not evaluated, because in C. graecum, flower and leaf development are concomitantly exhibited only during a two-month period, i.e., November and December.
Proline content in tubers of C. graecum showed a small but statistically significant increase from November to March, compared to the rest of the year. This accumulation may be driven by the low temperatures of the corresponding months and may be considered a stress-related response. An analogous profile was followed by its leaves, resulting in unchanged partitioning of proline between leaves and tubers, when leaves are coming through during the life-cycle of C. graecum; nevertheless, the greatest variation was found between petal and leaf concentrations. It has been published that C. graecum is a coldtolerant species [37,39]. The increased proline biosynthesis and accumulation may partly account for a cold hardiness feature in both tubers and leaves, due to its protectiveness regarding stress and radical scavenging role [40]. Concerning the latter, proline has been related to scavenging of hydroxyl radicals (OH) and possibly other ROS [41], while indirectly modifies the plant's antioxidant response through increasing the capacity of the involved enzymes, especially ascorbate peroxidase [22]. Additionally, proline accumulation patterns may have implications on nitrogen storage and partitioning, especially under stress conditions [22,27,42]. Proline pool has been reported to expand during transition phase, i.e., from vegetative to reproductive growth [43][44][45][46].
Ecophysiological traits of plant organs that are seasonally either renewed or shed may be a suitable criterion of plant's adaptation to environmental conditions. C. graecum survives the hot summer in a state of dormancy. C. graecum blooms in autumn, before leaf emergence. Thereafter, leaves grow and accumulate metabolic reserves throughout the wet and cool season, until the dormancy period, which begins in late spring. In geophytes, long days can initiate the transition to bud dormancy [47,48]. The summer dormancy protects plants from negative effects of water shortage and elevated temperatures on vegetative and reproductive organs, and forces their active development in a more favorable season. C. graecum is released from dormancy when the ambient temperatures decrease; hence, shifts from the vegetative to reproductive stage, and floral initiation and differentiation occur in the mature tubers [8,49].
Free proline accumulation in petals was remarkable and significantly increased compared to the other plant organs. Flowers exhibited a 2.5-to 5-fold enhanced proline content in comparison to tubers and 2-to 3-fold compared to leaves. The transportation of proline into the reproductive organs, even under non-stress conditions, has been repeatedly reported [49]. Corroborating our results, a 60-fold higher proline concentration was detected in tomato flowers than in all the vegetative tissues [50]. Enhanced proline content was also documented in petals of P. maritimum and was attributed to a requirement for osmotic adjustment, because this geophyte is exposed to dry and saline ambient environmental conditions [26,46]. Multiple explanations of proline accumulation in flowers have been published. For example, the increased proline content has been connected to the high yield of ATP resulting from its oxidation, thus considering proline a molecule well-suited to sustain high energy-demanding processes in reproductive tissues [44]. Low values of petal osmotic potential coincided with enhanced proline accumulation. Additionally, the protective role of proline, which was positively correlated with the turgor of petals of C. graecum, has been highlighted during floral developmental processes that include dehydration, as spontaneously occurring during pollen formation or embryogenesis [51,52]. Furthermore, proline may provide a convenient source of energy and nitrogen during immediate post-stress metabolism [46,49,53].

Research Site and Plant Phenology
The study was conducted in naturally occurring patches of Cyclamen graecum Link distributed in the campus of the National and Kapodistrian University of Athens in Greece (latitude: 37.9664, longitude: 23.756971, altitude 260 m), at the foothills of Hymettus Mountain, where travertine limestone appears along discontinuities of strongly fractured gray dolomite limestone; also, father soil characteristics, texture, and composition have been previously published [54,55]. Concerning perennial geophytes, most bulbs and tubers must reach a critical size before floral induction can occur [56]. In addition, large bulbs and tubers generally produce vigorous above-ground organs and/or many flowers. Therefore, the active and the dormant phenological stage ( Figure 2) were monitored, via detailed field observations in distinct niches of C. graecum [57], on a monthly basis for two consecutive years (2017 and 2018). The selected at random plants were growing under natural conditions; tubers, leaves, and flowers of C. graecum were sampled from a single stand of C. graecum surrounded by uniform Mediterranean phryganic vegetation [54], at monthly intervals during the course of a year, i.e., from September of 2018 to August of the next year (2019). The first flowers of C. graecum [58] appear in September, while the heart-shaped leaves are coming through in November, arising from the crown of the tubers [59]. Values of mean monthly precipitation and temperature, obtained from a meteorological enclosure, provided by the National Observatory of weather conditions in Greece, are presented in Figure 6a (annual data during the study period) and Figure 6b (multiannual data).
the next year (2019). The first flowers of C. graecum [58] appear in September, while the heart-shaped leaves are coming through in November, arising from the crown of the tubers [59]. Values of mean monthly precipitation and temperature, obtained from a meteorological enclosure, provided by the National Observatory of weather conditions in Greece, are presented in Figure 6a (annual data during the study period) and Figure 6b (multiannual data).

Determination of Total Soluble Sugar and Starch
Soluble sugars were extracted from dry, finely powdered samples (leaves, tubers, pedicels, petals) that were placed in 10 mL 80% ethanol (v/v), in a shaker, and the extracts were filtered using Whatman # 2 filter paper. Soluble sugar concentration was investigated colorimetrically, according to a modified phenol-sulphuric acid method [60,61], at 490 nm, using a spectrophotometer (Novaspec III + Spectrophotometer, Biochrom, Cambridge, UK). The determination of starch was made in the residue after the extraction of sugars, using the anthrone method [26,62]. D-glucose (Serva, Heidelberg, Germany) aqueous solutions were used for the standard curve. The values are expressed as mg g −1 d.w.

Determination of Proline
Free proline content was determined colorimetrically on 4 mL samples of the condensed fluid extracted from the plant material [63,64]. The extraction procedure from plant samples (finely powdered dried tubers, leaves, pedicels, and petals) and colorimetric determination were carried out as we have analytically published [26]. Dried, powdered samples were homogenized with aqueous sulphosalicylic acid (20 mL, 3% v/v), and the homogenate filtered through Whatman # 2 filter paper; 2 mL of the filtrate reacted with acid-ninhydrin solution (2 mL) and glacial acetic acid (2 mL) in test tubes, which were placed in a water bath at 100 • C for 1 h, and the reaction terminated in an ice bath. After cooling, the reaction mixture was extracted with 4 mL toluene and homogenized in a vortex. The chromophore containing the toluene was aspirated from the aqueous phase and the absorbance was read at 520 nm; immediately after, the terminated reaction in glass tubes placed in an ice bath, using toluene as a blank sample and the spectrophotometer mentioned in paragraph 5.2. The proline concentration was estimated using a standard curve of relevant L-proline solutions (Serva, Heidelberg, Germany) and calculated on a dry weight basis.

Determination of Water Status
Petal water potential (Ψ) was measured psychometrically on 6 mm diameter fresh discs (five replicates) from fully expanded petals, which were placed in five C-52 psychrometric chambers (Wescor Inc., Logan, UT, USA) attached to a dew point psychrometer (HR-33T, Wescor Inc.) using the psychrometer switchbox (PS-10, Wescor); the time required for equilibration between the water vapor pressure of leaf sample and that of the psychrometer chamber was 2 h. The osmotic potential (Ψ s ) was measured using the same leaf discs after freezing and thawing [65,66]. Turgor pressure (Ψ p ) was calculated as the algebraic difference between Ψ and Ψ s . The relative water content (RWC) of fully expanded leaves was determined according to the disc method [29], using the equation RWC (%) = [(FW − DW)/(TW − DW)] × 100, where: FW is the sample fresh weight, TW is the sample turgid weight, and DW is the sample dry weight.

Statistical Analysis
The results are presented as mean ± Standard Error (SE). In order to determine differences in the studied parameters of plant parts of C. graecum, a two-way analysis of variance (ANOVA) was performed on the studied parameters at p < 0.05 and the Duncan's multiple range test was applied for comparing the means. All statistical tests were performed using the SPSS statistical v. 23.0 (SPSS Inc., Chicago, IL, USA). Regression analysis was used to determine relationships among results obtained by plant tissues of C. graecum and precipitation.

Conclusions
The life form of C. graecum is characterized by two phenological stages in the course of a year, the active phase (from flower emergence in September to leaf senescence in April), and the dormant phase spanning the prolonged drought period, when above-ground plant parts are not exposed to the severity of summer in the eastern Mediterranean. Partitioning patterns of soluble sugars, starch, and free proline in above-and below-ground parts of C. graecum contribute to the maintenance of its annual rhythm and phenophases in fluctuating environmental conditions. The remarkable concentration of proline in petals, in comparison to other plant parts during autumn, seems to be associated with the maintenance of their turgor; without turgor, the exposed petals to ambient environmental conditions of the sharply reflexed corolla of C. graecum could not be standing so firm and erect. The leaf relative water content was found lower than the typical values of turgid and transpiring leaves; this may indicate that leaves of C. graecum subjected to ambient conditions are not susceptible to low temperatures. However, further work will be required to fully test this hypothesis.