Documenting Greek Indigenous Germplasm of Cornelian Cherry (Cornus mas L.) for Sustainable Utilization: Molecular Authentication, Asexual Propagation, and Phytochemical Evaluation

Wild-growing Cornelian cherries (Cornus mas L., Cornaceae) are well-known native fruits in Greece since ancient times that are still consumed locally nowadays. Modern research has highlighted the value of Cornelian cherries as functional food with exceptional health benefits on account of the fruits’ biochemical profile. However, apart from local consumption directly from wild growing individuals, Greek native C. mas populations have not yet been investigated or sustainably utilized. A multifaceted evaluation was conducted herein including authorized collection-documentation, taxonomic identification, and molecular authentication (DNA barcoding), asexual propagation via cuttings and phytochemical evaluation (multiple antioxidant profiling) of neglected and underutilized Greek native C. mas germplasm sources. Successive botanical expeditions resulted in the collection of 18 samples of genotypes from distant C. mas populations across different natural habitats in Greece, most of which were DNA fingerprinted for the first time. Asexual propagation trials revealed high variability in rooting frequencies among Greek genotypes with low (<25%), average (25–50%), and adequate propagation potential (>50%) using external indole-3-butyric acid (IBA) hormone application on soft- or hard-wood cuttings. The comparative phytochemical evaluation of the studied Greek genotypes showed significant potential in terms of antioxidant activity (>80% radical scavenging activity in 13 genotypes), but with variable phenolic content (47.58–355.46 mg GAE/100 g), flavonoid content (0.15–0.86 mg CE/100 g), and vitamin C content (1–59 mg AAE/100 g). The collected material is currently maintained under ex situ conservation for long-term monitoring coupled with ongoing pilot cultivation trials. The pivotal data create for the first time a framework for the sustainable utilization of Greek native C. mas germplasm as a superfood with significant agronomic potential.


Introduction
Apart from widely used crop varieties, phytogenetic resources also include wildgrowing plant species which are often neglected or underutilized, especially in biodiversityrich areas [1]. Such germplasm resources involve a wide variety of plant species, including small fruit trees of potentially high alimentary value, relating to nutritional health benefits, but also pharmaceutical value [2][3][4][5][6]. Local native fruit species can be an important source of natural food products rich in antioxidants such as polyphenols with known importance for human health [7][8][9]. The natural heritage of Greece and its rich biodiversity at all levels offer new possibilities for evaluating and utilizing valuable wild germplasm such as small stone fruits and berries with high nutritional and medicinal (in one word nutraceutical) value [6,10]. Prior to domestication and sustainable exploitation of wild germplasm resources of interest, multifaceted research approaches are required in terms of taxonomic validation and molecular authentication of wild plant material, agronomical assessment propagation-wise, and comprehensive phytochemical evaluation aiming at the selection of promising genotypes with high potential for further applied research and future breeding. To this end, Greek native Rosa canina and Sambucus nigra germplasms constitute recently developed example cases [6,10].
Cornelian cherry (Cornus mas L., Cornaceae) is a rather common and wild-growing deciduous shrub or occasionally a small tree 2-4(-6) m tall in scrub and woodlands of central and southeastern Europe and western Asia, often occurring in ravines or near streams (areas with sufficient rainfall) from low (100-200 m) to intermediate and higher altitudes (800 m, occasionally up to 1700 m) [11]. In Greece, Cornelian cherry is a traditionally wellknown native fruit tree that has been consumed locally for centuries and it has been known since ancient times, i.e., the Trojan horse in Homeric times was believed to be a C. mas woodcraft [12]. The trees bloom by the end of winter and in early spring and set fruits (ellipsoid to broadly cylindrical drupes 12-15 mm long, becoming red and cherry-like) in late summer through fall. Cornelian cherry fruits (both wild-growing and cultivated) and their food derivatives (e.g., jams, jellies, juice) contain antioxidants, phenolic compounds, iron, potassium, vitamin C, flavonoids, and many other substances of high nutritional value [13][14][15][16][17]. In addition, C. mas fruits to date have validated pharmaceutical value in terms of free radical scavenging potential among others, resulting in several health benefits including antimicrobial, antidiabetic, anti-inflammatory, anticancer, and cardioprotective activity; these assets render C. mas fruits as functional food products and as 'superfood' with intensifying relevant research over recent years [18][19][20]. Apart from the flesh of the fruits, the endocarp of C. mas drupes has also been demonstrated to have nutraceutical potential as a source of bioactive compounds with strong antioxidant activity [21]. Sustainable utilization efforts of C. mas germplasm have been attempted in eastern European countries with promising results [22][23][24]. In more recent studies in the same area, the phytochemical evaluation of C. mas domesticated germplasm (cultivars and/or hybrids) has been conducted [22]. Furthermore, C. mas germplasm has been characterized in terms of the nutritional value of the fruits across a wider spectrum of its distribution range [25][26][27][28] and the results showed the nutritional superiority of wild-growing germplasm [29]. However, in these studies no assessment was included regarding the native C. mas wild-growing genotypes occurring in Greece.
To support classical taxonomic identification and to enable the establishment of a distinct genetic identity, molecular authentication can be performed through novel DNA barcoding and bioinformatic analysis methods in selected plant materials collected from natural habitats [30]. DNA barcoding as a tool for molecular authentication of plant germplasm has been greatly developed and to date is being widely used for many medicinal plant species and phytogenetic resources [6,10,[31][32][33][34][35]. There are also reports of DNA barcodes being successfully used in identification of ancient DNA (aDNA) of C. mas from fossils [36]. However, such molecular tools are still underused in authenticating native C. mas germplasm of different regions. To date, wild-type populations of Cornelian cherry (C. mas) from several parts of the world have been successfully propagated via cuttings in the past with the use of external hormone application on hardwood and soft wood cuttings taken from mature individuals growing in the wild [37,38]. A popular hormonal substance that has been used in the past is indole-3-butyric acid (IBA) [39,40], frequently achieving high rooting rates.
In this framework, the study herein was focused on the collection and multifaceted documentation of C. mas plant material from geographically separated Greek populations (different genotypes) with the aim to provide: (1) molecular authentication of the population samples via DNA barcoding; (2) asexual propagation protocols for the collected genotypes via propagation trials using cuttings (dormant hardwood twigs, fresh softwood plant parts) facilitating the ex situ conservation and evaluation of the collected germplasm; and (3) comparative phytochemical evaluation of their fruits in terms of nutraceutical properties (total phenolic content, antioxidant activity, total flavonoids, and vitamin C content) to assess their potential as germplasm sources for artificial selection of genotypes and future breeding efforts. The overall work provided first-time insight into Greek native C. mas (Cornelian cherry) germplasm and these efforts are aimed at paving the way for its sustainable utilization as a superfood with significant agronomic potential.

Molecular Authentication of Greek Native Cornus mas Genotypes
BLAST1 and distance-based methods were selected to validate the authentication efficiency of ITS2 for the selected Greek native Cornus mas genotypes. The ITS2 barcode with BLAST1 showed a high competence (97% and 100%) in sample identification at species and genus levels, respectively. The ITS2 barcode with the DISTANCE method showed almost similar identification efficiency (98%) at the species level. Thus, barcode ITS2 using the NJ tree method was proved able to distinguish Greek native C. mas genotypes from other genotypes of different origin, and similarly, from other Cornus spp. not present in Greece ( Figure 1A). The neighbor-joining (NJ) phylogenetic tree obtained from DNA barcoding application with the ITS2 region discerned two main groups among the samples of Cornus spp. used herein (n = 21), and clearly classified the Greek native C. mas genotypes of this study as distinct sub-group with respect to other samples of C. mas of different origins that were sourced from databases ( Figure 1A). The nucleotide differences in Greek genotypes are depicted in Figure 1B. The separation of the genotypes in Figure 1A presents similarity to an extent with the geographical separation of the respective habitats since genotypes GR-1-BBGK-19,195, GR-1-BBGK-19,197, GR-1-BBGK- 19,198, and GR-1-BBGK-19,190 coupled with genotype GR-1-BBGK-19,196 originate from areas of the same prefecture, whereas genotype GR-1-BBGK-19,72 is both genetically and geographically further apart ( Figure 1A). The same holds true for genotype GR-1-BBGK-19,502 which is geographically separated coming from the lowest altitude. The bootstrap values seem to further validate this classification scheme. Despite the fact that evolutionary relationships may also be analyzed through the neighbor-joining tree, the key function applied herein was to repeatedly evaluate bootstrap values as a measure of informed distinction of the Greek native germplasm (see distinct clades). The results of this study outlined the ITS2 gene as an efficient tool (100%) regarding the distinction of the species in concern (C. mas) among other Cornus spp. (see monophyletic clusters).  The distinct genotypes of this study are highlighted with blue.

Altitude
In addition to the above results, significant year-to-year variations were observed in genotypes that were measured for two consecutive years, especially in TPC. Particularly, genotype GR-1-BBGK-19,190 showed a drop in TPC from 304.73 mg GAE/100 g in 2019 to 49.29 mg GAE/100 g in 2020 coupled with a drop in TF from 0.73 to 0.22 mg CE/100 g ( Table 1, p < 0.05). On the contrary, genotypes GR-1-BBGK-19,633 and GR-1-BBGK-19,638 showed an increase in TPC between 2019 and 2020 from 52.31 to 195.2 mg GAE/100 g and from 29.93 to 337.14 mg GAE/100 g, respectively, with the latter showing also a significant increase in AA (Table 1, p < 0.05).

Propagation of Greek Native Cornus mas Genotypes with Cuttings
A variation in rooting capacity was observed between different genotypes of C. mas. Rooting frequencies varied from 1.19% in genotype GR-1-BBGK-19,641 with 6000 ppm IBA/softwood cuttings in summer to 69.93% in genotype GR-1-BBGK-19,638 with 10,000 ppm IBA/softwood cuttings in late summer which was the highest rooting capacity observed (p < 0.05). The next best rooting capacity (58.33%) was observed in genotype GR-1-BBGK-19,753 with 4000 ppm IBA/softwood cuttings in early autumn (Table 3, p < 0.05). Hardwood, dormant cuttings during the winter presented generally low rooting rates which took months to be reached since cuttings remained under mist throughout winter and started to root in the following spring. The highest rooting frequency observed within this group was 20.93% (p < 0.05) in genotype GR-1-BBGK- 19,198. For the rest of the genotypes that were tested via softwood non-dormant cuttings during the summer through early autumn, rooting was still diverse, but more cases of higher rates were found compared to genotypes tested in winter, with three and two genotypes presenting >30% and 50% rooting, respectively (Table 3, p < 0.05, Figure 2). The symbols † and ‡ denote the highest rooting frequencies for hardwood and softwood cuttings, respectively, following pairwise comparisons of the observed rooting frequencies via Pearson X 2 tests. All cases were tested against a control treatment with no hormone application and no rooting.

Molecular Authentication of Greek Native Genotypes of Cornus mas
In general, DNA barcoding may offer support to classical morphological identification of samples and insight into phylogenetic relationships of closely related species; thus it is an efficient method for the discernment of various genotypes independently from the stage of plant development [6,10]. Herein, we provide the first-ever report regarding the molecular authentication of Greek native germplasm of Cornus mas, with the NJ (Neighbor-Joining) tree classification obtained from the ITS2 barcoding discerning clearly the DNA fingerprints of the Greek genotypes. Undoubtedly, more genotypes from different habitats in different regions of Greece should be evaluated to further confirm this distinctiveness. Regardless, as reported herein, the ITS2 gene can be an effective marker for the identification of Cornus spp. and of different genotypes thereof; thus, offering to deciphering their evolutionary relationships.

Nutraceutical Potential of Greek Native Genotypes of Cornus mas
The current work presents for the first time comprehensive phytochemical data for an extended range of Greek native wild-growing Cornus mas genotypes assessing their potential as a functional food or superfood for ex situ conservation and future breeding efforts. The parameters assessed herein revolve around human oxidative stress and particularly plant secondary metabolites with known free radical scavenging activity such as phenolic compounds and flavonoids coupled with vitamin C content [41]. The results showed that at least five Greek genotypes with significant nutraceutical potential can be

Multifaceted Evaluation of Greek Native Cornus mas Genotypes
An overview of the sustainable exploitation potential of the native C. mas genotypes assessed in this study is summarized in Table 4 in a multifaceted way based on the obtained molecular authentication results, the propagation success achieved, and the phytochemical profiles assessed. From the effectively authenticated genotypes, GR-1-BBGK-19,72 showed very high antioxidant activity and average propagation potential (Table 4, Figure 2) and could be prioritized for further research. However, genotypes GR-1-BBGK-19,190 and GR-1-BBGK-19,195 also showed high antioxidant activity but it is unclear from the current data whether the low propagation success observed was due to genotype effect or due to winter hardwood cuttings since these genotypes were only tested during the winter in contrast with GR-1-BBGK-19,72 (Table 1, Table 3, Table 5). As far as the rest of the genotypes are concerned, genotype GR-1-BBGK-19,638 stands out with very promising phytochemical potential and high propagation success and, as such, this genotype merits further investigation. Another genotype that showed a promising potential is GR-1-BBGK-19,753 with high propagation success and strong antioxidant activity (Table 3, Figure 2). Table 4. Multifaceted evaluation of Greek native Cornus mas genotypes based on molecular authentication effectiveness (Figure 1), fruit phytochemical potential expressed as antioxidant activity (AA, %RSA: low ≤50, average 51-70, high 71-90, very high >90), total phenolic content (TPC, mg GAE/100 g: low ≤50, average 51-100, high 101-200, very high >200) and vitamin C content (mg AAE/100 g: low ≤30, average 31-50, high >50) (Table 1), and asexual propagation potential expressed as hormone-induced rooting under the most successful application (very low < 10%, low 11-30%, average 31-55%, or high >55%), (Table 3).

Molecular Authentication of Greek Native Genotypes of Cornus mas
In general, DNA barcoding may offer support to classical morphological identification of samples and insight into phylogenetic relationships of closely related species; thus it is an efficient method for the discernment of various genotypes independently from the stage of plant development [6,10]. Herein, we provide the first-ever report regarding the molecular authentication of Greek native germplasm of Cornus mas, with the NJ (Neighbor-Joining) tree classification obtained from the ITS2 barcoding discerning clearly the DNA fingerprints of the Greek genotypes. Undoubtedly, more genotypes from different habitats in different regions of Greece should be evaluated to further confirm this distinctiveness. Regardless, as reported herein, the ITS2 gene can be an effective marker for the identification of Cornus spp. and of different genotypes thereof; thus, offering to deciphering their evolutionary relationships.

Nutraceutical Potential of Greek Native Genotypes of Cornus mas
The current work presents for the first time comprehensive phytochemical data for an extended range of Greek native wild-growing Cornus mas genotypes assessing their potential as a functional food or superfood for ex situ conservation and future breeding efforts. The parameters assessed herein revolve around human oxidative stress and particularly plant secondary metabolites with known free radical scavenging activity such as phenolic compounds and flavonoids coupled with vitamin C content [41]. The results showed that at least five Greek genotypes with significant nutraceutical potential can be distinguished, namely GR-1-BBGK-19,72, GR-1-BBGK-19,190, GR-1-BBGK-19,195, GR-1-BBGK-19,638, and GR-1-BBGK-19,753 (Table 4). Similarly to the current results, a wide range of TPC of the fruits was detected in studies dealing with wild-growing C. mas germplasm in Romania, coupled with significant variability among genotypes in other fruit phytochemical traits [42,43]. Some similarities can also be found between C. mas wild-growing genotypes of Serbia with those studied herein in terms of vitamin C content that also show higher sugar content due to higher fruit maturity index at the time of collection [15].
Although variable among genotypes, the phytochemical properties of the Greek germplasm are generally similar with both wild-growing and cultivated C. mas genotypes reported from countries at a similar latitudinal range as Greece such as Turkey [13]. However, studies on Central European genotypes of C. mas cultivated in higher latitudes have shown higher antioxidant activity (AA) of the fruits that ranged from 3.30 to 9.54 g AAE/1000 g, which implies an interaction of genotype with climatic conditions affecting fruit phytochemical profile [14]. Evidence regarding the effects of the climatic conditions in interaction with genotype on fruit phytochemical profile can also be seen through the significant correlation of total dissolved solids (TDS) with vitamin C content observed among genotypes herein, since TDS is physiologically connected to climatic factors [14]. In a more recent study concerning an Italian cultivated genotype of C. mas, total phenolic content (TPC) was found at 196.68 mgGAE/100 g [44], which is similar to some genotypes assessed herein and even lower than three of the studied genotypes, while vitamin C content was at similar ranges. Recently, the phytochemical profile of fruits was comparatively evaluated between cultivars of C. mas, genotypes of the Chinese endemic Cornus officinalis Siebold and Zucc., and hybrids thereof (C. mas X C. officinalis). C. mas cultivars in that study have shown a similar TPC range with the studied Greek genotypes apart from one cultivar which was higher, yet the TPC and AA of the hybrids was generally higher, indicating the significance of conservation of C. mas germplasm stocks for breeding programs [22]. The nutraceutical potential of native genotypes has been similarly assessed on other Greek germplasm resources such as, for example, Rosa canina [10] with slightly higher potential of AA and TPC detected and comparable to some extent with that of C. mas, but with very high content of vitamin C for R. canina [10].
The climatic conditions (most prominently temperature along with sunshine) during the last stages of fleshy fruit ripening in cornelian cherries may affect acid reduction and sugar increase, which in turn affects biosynthesis of secondary metabolites [45,46]. As such, the climatic conditions of the natural habitats of wild populations on one hand and the stage of fruit collection and fruits' ripening status on the other hand are considered as significant factors in terms of comparative phytochemical evaluations. However, in this study no significant correlations were observed between the fruit phytochemical properties measured and the altitude from which they were collected in the wild or their maturity index determined as the ratio of sugar content to malic acid content. This observation indicates that the variability of phytochemical properties observed among Greek native genotypes of C. mas may be attributed to genetic factors rather than timing of fruit harvest or altitudinal differences between collection sites. Nevertheless, further ecological profiling work in terms of correlation studies with more environmental/topoclimatic parameters and more fruit phenological traits on Greek C. mas wild populations is suggested.

Propagation Potential of Greek Native Genotypes of Cornus mas
A further component of the multifaceted evaluation of wild Greek C. mas genotypes investigated herein is the asexual propagation via cuttings which was conducted for the first time in Greek germplasm. Similarly to fruit phytochemical data, the genotypes of C. mas tested showed variable rooting capacity with a number of them being below the commercially accepted threshold [47]. In all cases, however, external hormone application was necessary to achieve even low rooting frequencies which are in agreement with similar studies [38,39,48]. Hardwood dormant cuttings tested in the current study remained under mist for the duration of winter and started to root the following spring giving low rooting rates (<25%) under 10,000 ppm IBA treatment. This observation concurs with similar studies on cutting propagation of C. mas genotypes in other countries where softwood cuttings surpassed hardwood cuttings under the 10,000 ppm IBA treatment [38]. The poor results on hardwood cuttings indicate that it is not economically efficient to produce new plants via winter dormant cuttings [37,40], a fact that also applies for the Greek germplasm. Softwood cutting material with a small degree of lignification has known advantages in rooting quality with external hormone utilization [49], producing higher rooting rates in Cornus alba [50]. Even in other genera, cutting type affected by the status of mother's plant growth has been linked to rooting capacity and quality [51][52][53]. Consequently, since only two of the selected genotypes evaluated herein showed appreciable propagation potential (>50% rooting in genotypes GR-1-BBGK-19,638 and GR-1-BBGK-19,753) with softwood cuttings (Table 3), further research is required to explore pathways on improving rooting capacity but also to investigate the relationships between cutting type and rooting capacity and quality in more detail. Additionally, further research is proposed on the correlation of rooting factors with early plant establishment and survival in C. mas propagation since such a correlation has been shown to be significant in other Greek native germplasm resources such as Sambucus nigra [6].
Finally, asexual propagation through grafting has been attempted on European C. mas germplasm with positive results [54], showing that successful grafting in C. mas can enhance growth and development of the scion [55]. For the Greek native C. mas genotypes studied herein, the method of grafting a genotype with high phytochemical potential but low rooting capacity onto another genotype with improved rooting capacity may provide a good option in dealing with difficult-to-root genotypes but with valuable fruit traits. However, further research is required to systematically test this strategy.

Collection and Documentation of Plant Material
A plethora of botanical expeditions took place covering a wide range of geographically distant and altitudinally different natural habitats of C. mas across Northern Greece reached at consecutive stages across two years (Table 5). Targeted and variable types of plant material were collected (Table 5)

DNA Isolation
A standardized commercial DNA extraction kit (Nucleospin Plant II, Macherey-Nagel) was used for DNA extraction following the manufacturer's instructions using approximately 30 mg of dried leaf sample from each C. mas genotype that was previously ground in liquid nitrogen.
A standardized commercial DNA extraction kit (Nucleospin Plant II, Macherey-Nagel) was used for DNA extraction following the manufacturer's instructions using approximately 30 mg of dried leaf sample from each C. mas genotype that was previously ground in liquid nitrogen.

Polymerase Chain Reaction (Pcr) Amplification and Sequence Analysis
PCR amplification was conducted according to [57] using one primer set of the nuclear ITS2 barcode region [58]. The resulting PCR products for each genotype were consecutively sequenced using an automated ABI 3730 sequencer (PE Applied Biosystems), in two directions of each fragment with a Big Dye terminator v3.1 Cycle sequencing kit (PE Applied Biosystems, Foster City, CA, USA). The sequences were aligned using the CLUSTAL W program.

Molecular Data Analysis
Following the results of the sequence analysis, the molecular authentication of the Cornus mas genotypes studied was conducted using three methods: (i) evaluation against the nucleotide database at NCBI using the Basic Local Alignment Search Tool (BLAST); (ii) using maximum-likelihood models for the genetic divergence method; and (iii) tree topology analysis using the Neighbor-Joining (NJ) method based on different loci in MEGAX with the K2P distance model and 1000 bootstrap replications. The generated ITS2 DNA barcoding sequences (without primers used for PCR amplification) were deposited to the NCBI-Genbank (https://www.ncbi.nlm.nih.gov/BankIt/, accessed 5 May 2022) under the accession numbers MZ35480-MZ35488.

Phylogenetic Relationships
The phylogenetic relationship of Cornus spp. was inferred using the Neighbor-Joining (NJ) method [59]. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) are shown next to the branches [60]. The evolutionary distances were estimated using the Maximum Composite Likelihood (MCL) method [61]. All ambiguous positions were removed for each sequence pair (pairwise deletion option). The phylogenetic dendrogram was constructed using the MEGA X software [62].

Propagation Trials
Depending on the propagation material obtained from each expedition, a variety of targeted experiments were conducted using different external hormone application treatments of indole-3-butyric acid (IBA) [50,63] and different cutting types taken at different seasons from varying stages of mother plant growth (Table 5). Cuttings were set for rooting in propagation trays under mist where relative humidity (RH) was maintained at >85% within a greenhouse at ambient temperature. The substrate used was peat (Klasmann, KTS 1):perlite at 1:3 v/v. Cuttings were attended weekly to assess their rooting capacity. The produced mother plants were kept ex situ at the laboratory's nursery in the grounds of IPB and GR under ambient conditions for plant adaptation. The plants were watered regularly and were grown in 3 L pots using a mixture of peat (Klasmann, KTS 2) and perlite (3:1, v/v).

Phytochemical Analysis of Cornus mas Fruits
A modified method described in [64] was used for preparation of the extracts. An appropriate volume of MeOH/H 2 O (60:40) was mixed with 2-5 g of homogenized sample and was centrifuged at 4000rpm at 4 • C. The collected supernatant was made up to 20 mL volume and was used for the determination of total phenolic content (TPC), total flavonoids (TF), and antioxidant activity (AA). For the determination of TPC, phenolic extract 0.20 mL along with 2.3 mL of H 2 O and 0.25 mL of Folin-Ciocalteu reagent were added in a volumetric flask [64] in which, after 3 min, 0.50 mL of 20% Na 2 CO 3 was added, and the volume was made up to 5 mL. The above solution was stored in a dark place for 2 h and the absorbance was measured at 725 nm against blank solution. The calculation of TPC was conducted using a standard curve of gallic acid at various concentrations giving the results expressed as gallic acid equivalents (GAE)/100 g of sample. All analyses were carried out in triplicate.
A modified method for the determination of TF was used according to [65]. In a test tube, 5 µL of the above extract were added along with 3270 µL of H 2 O and 75 µL of 5% NaNO 2 , stirred, and stored in the dark for 5 min which was then added with 150 µL of 10% AlCl 3 -6H 2 O, mixed, and stored in the dark for a further 6 min. Consequently, it was added with 500 µL of 1 M NaOH and the absorbance was measured at 510 nm against H 2 O as blank. The calculation of TF was conducted using a standard curve of catechin at various concentrations giving results expressed as catechin equivalents (CE)/100 g of sample. All analyses were carried out in triplicate.
A modified method for the determination of AA was employed described in [66]. In a 5 mL plastic cuvette, 0.1 mL of phenolic extract was added along with 2.9 mL 0.10 mM (2,2-diphenyl-1-picrylhydrazyl (DPPH)) in MeOH, stored in the dark for 15 min and then the absorbance was measured at 517 nm against MeOH as blank. The control sample was prepared using 0.10 mM DPPH in MeOH. The percentage of radical scavenging activity (%RSA) was carried out in triplicate and was calculated using the following equation: where A o = absorbance of control sample. A s = absorbance of the sample after 15 min of incubation. A modified method for the determination of vitamin C presented in [67] was used. A mixture of homogenized sample (2-5 g) and 5 mL of 4.5% w/v metaphosphoric acid (MPA) solution was stirred and centrifuged at 8000 rpm at 4 • C for 20 min. The supernatant (1 mL) was taken and diluted up to 10 mL with 4.5% MPA solution and it was filtered through 0.45 µm polyethersulfone filters. The vial was covered with aluminum foil to prevent oxidation of ascorbic acid and stored at 4 • C until HPLC-DAD analysis. HPLC-DAD analysis conditions: Column (Agilent Eclipse XDB-C18) 4.6 mm × 150 mm, 5µm, elution solvent: aqueous 0.005 M H 2 SO 4 solution at a flow rate of 0.5 mL/min (isocratic) and wavelength 245 nm. A standard curve of ascorbic acid at various concentrations was used for vitamin C content calculation which gave results expressed as ascorbic acid equivalents (AAE)/100 g of sample.
Sugar content of fruit samples was measured via Brix analysis ( o Bx), and the maturity index (MI) of fruits was calculated as the ratio of sugar content in • Bx to malic acid (MA) content expressed as grams of MA per 100 g.
All analyses were carried out in triplicate.

Experimental Design and Statistical Analysis of Propagation and Phytochemical Data
The propagation trials followed a complete randomized design. The number of replicate cuttings per treatment varied according to the volume of material obtained from each expedition (Table 5). Targeted IBA hormone application treatments were applied ranging from 2000 to 10,000 ppm depending on the season and whether the cuttings were softwood or hardwood, respectively (Table 5). Each trial included a control with an equal number of replicate cuttings. The rooting frequencies obtained were compared through pairwise Pearson Chi-Square tests.
For the phytochemical data that were measured in triplicate, a mean coupled with its standard deviation (±S.D.) was calculated in each case and means were compared using Tukey's HSD post hoc test. In addition, the phytochemical data were subjected to Pearson's correlation coefficient analysis to determine the correlations between the different fruit phytochemical traits measured along with the differences in altitude between the natural habitats of C. mas that collection occurred in. All analyses were conducted using the IBM-SPSS 23.0 software.

Conclusions
In conclusion, the multifaceted evaluation that was conducted provides a first depiction of the sustainable exploitation potential of Greek native Cornus mas genotypes. All genotypes collected from the wild are under ex situ conservation at the IPB and GR for future monitoring, since juvenile-mature correlations are known in perennial crops from the literature [68,69]; such aspects should be taken into account for future long-term breeding programs. The transition from the juvenile to the mature (producing) stage followed by several phenological and developmental changes was found to vary among genotypes mainly in forest species but also in cultivated deciduous tree species with stone fruits such as apples [69]. Consequently, further work on molecular authentication, ecological profiling, and phytochemical profiling is proposed coupled with further research on propagation. In addition, the long-term monitoring of the current Greek genotypes is needed, and in fact, pilot cultivation trials of the genotypes prioritized herein have been established (ongoing process). The data obtained in the current study along with the conservation of the plant material collected can serve as a basis for future breeding efforts, creating for the first time a framework for the sustainable utilization of Greek native C. mas germplasm as a superfood with significant agronomic potential.