Characterization of Some Cichorium Taxa Grown under Mediterranean Climate Using Morphological Traits and Molecular Markers

The verification of taxonomic identities is of the highest significance in the field of biological study and categorization. Morpho-molecular characterization can clarify uncertainties in distinguishing between taxonomic groups. In this study, we characterized five local taxa of the genus Cichorium using morphological and molecular markers for taxonomic authentication and probably future genetic improvement. The five Cichorium taxa grown under the Mediterranean climate using morphological traits and molecular markers showed variations. The examined taxa showed a widespread range of variations in leaf characteristics, i.e., shape, type, texture, margin, and apex and cypsela characteristics i.e., shape, color, and surface pattern. The phylogenetic tree categorized the Cichorium intybus var. intybus and C. intybus var. foliosum in a single group, whereas C. endivia var. endivia was grouped separately. However, C. endivia var. crispum and C. endivia subsp. pumilum were classified as a cluster. The recorded variance between classes using the molecular markers SCoT, ISSR, and RAPD was documented at 34.43%, 36.62%, and 40.34%, respectively. Authentication using molecular tools proved the usefulness of a dichotomous indented key, as revealed by morphological identification. The integrated methodology using morphological and molecular assessment could support improved verification and authentication of the various taxa of chicory. It seems likely that the Egyptian chicory belongs to C. endivia subsp. pumilum.

The Egyptian chicory ("Sreece" according to its local Arabic name) belongs to the C. endivia sub-species pumilum in the Asteraceae family. However, several published articles from Egypt still incorrectly assume that the Egyptian chicory belongs to the C. intybus species [38][39][40]. The integrated approach using micro-macro morphological assessment and molecular techniques could help to improve authentication and verification of the species and taxa. With the lack of extensive sampling of several genera and representative species, the family's phylogeny and diversifications have been hampered by the limited availability of research covering species and varietal diversity, along with the high resemblance among species.
This study highlights the morphological and molecular characteristics of five taxa of the genus Cichorium through assessment and discrimination to determine the relationships among taxa. The micro-and macro-morphological data generated a relationship among the taxa of Cichorium, while the PCR-based markers provided information on Cichorium's genetic relatedness. The goal of this study is to present analyses to accurately classify the studied chicory species. In order to resolve the classification ambiguity, we offer a robust argument by documenting morphological and genetic differences between the C. endivia and C. intybus species of chicory.

Leaf Morphology
The leaves of the studied Cichorium taxa have the following characteristics in common: they are simple, reticulate, pinnate, glabrous, and exstipulate, and have symmetrical epulvinate bases (Table 1 and Figure 1). The shape of the studied leaves is obovate in C. endivia var. crispum, oblancelate in C. endivia subsp. pumilum, and spathulate in C. intybus var. intybus, C. intybus var. foliosum, and C. endivia var. endivia. The leaves are petiolate in C. intybus var. intybus, C. intybus var. foliosum, and C. endivia subsp. pumilum but, they are sessile in C. endivia var. endivia and C. endivia var. crispum. The leaf blade is simple in all of the studied plants, except C. endivia var. crispum, whose leaf blade is pinnately lobed. Margins of the leaves are dentate in most of the examined taxa, as in C. intybus var. intybus, C. endivia var. endivia, and C. endivia var. crispum, but they are finely dentate in C. intybus var. foliosum and C. endivia subsp. pumilum. All of the investigated plants have obtuse leaf apex shapes, as in Cichorium. The midrib is distinct in all plants except C. endivia var. crispum. Generally, within each taxon, remarkable variability was not noticed.

Cypsela Morphology
Details of the micro-morphological characteristics of the cypsela of Cichorium are presented in Figures 2 and 3 and Table 1. The cypsela surface is smooth and sometimes rough, and the shape of the hilum is circular. The anticlinal wall shape is straight, and there is pappus persistence in all studied taxa. Fruits of Cichorium are cypsela (achene). The shape is oblong in C. intybus var. intybus, C. endivia var. endivia, and C. endivia var. crispum, but oblong-obovate in C. intybus var. foliosum and C. endivia subsp. pumilum. The color ranges from creamy and shiny to black: C. intybus var. intybus is creamy, C. intybus var.
foliosum and C. endivia var. endivia range from creamy shiny to dark brown and creamy, C. endivia var. crispum ranges from pale, creamy, and shiny to creamy with a black point, and C. endivia subsp. pumilum is creamy shiny with a few dark brown spots. The surface pattern of C. intybus var. intybus and C. intybus var. foliosum is sulcate papillate, that of C. endivia var. endivia is weak sulcate papillate, that of C. endivia var. crispum is ruminate sulcate, and that of C. endivia subsp. pumilum is weak ruminate-sulcate papillate. The anticinal wall is raised in C. intybus var. intybus and C. intybus var. foliosum, and slightly raised in C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum. Periclinal walls are concave in C. intybus var. intybus and C. intybus var. foliosum, but only slightly concave in C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum. Pappus bristles may be scabrous scales in C. intybus var. intybus and C. intybus var. foliosum and paleaceous scales to form a crown in C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum. Pappus length is short in C. intybus var. intybus, C. intybus var. foliosum, and C. endivia subsp. pumilum, but long in C. endivia var. endivia and C. endivia var. crispum. sented in Figures 2 and 3 and Table 1. The cypsela surface is smooth and sometimes rough, and the shape of the hilum is circular. The anticlinal wall shape is straight, and there is pappus persistence in all studied taxa. Fruits of Cichorium are cypsela (achene). The shape is oblong in C. intybus var. intybus, C. endivia var. endivia, and C. endivia var. crispum, but oblong-obovate in C. intybus var. foliosum and C. endivia subsp. pumilum. The color ranges from creamy and shiny to black: C. intybus var. intybus is creamy, C. intybus var. foliosum and C. endivia var. endivia range from creamy shiny to dark brown and creamy, C. endivia var. crispum ranges from pale, creamy, and shiny to creamy with a black point, and C. endivia subsp. pumilum is creamy shiny with a few dark brown spots. The surface pattern of C. intybus var. intybus and C. intybus var. foliosum is sulcate papillate, that of C. endivia var. endivia is weak sulcate papillate, that of C. endivia var. crispum is ruminate sulcate, and that of C. endivia subsp. pumilum is weak ruminate-sulcate papillate. The anticinal wall is raised in C. intybus var. intybus and C. intybus var. foliosum, and slightly raised in C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum. Periclinal walls are concave in C. intybus var. intybus and C. intybus var. foliosum, but only slightly concave in C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum. Pappus bristles may be scabrous scales in C. intybus var. intybus and C. intybus var. foliosum and paleaceous scales to form a crown in C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum. Pappus length is short in C. intybus var. intybus, C. intybus var. foliosum, and C. endivia subsp. pumilum, but long in C. endivia var. endivia and C. endivia var. crispum.

Epidermal Characteristics
In this study, five taxa of Cichcorium were investigated for their epidermal characters and trichomes, in order to determine the essential characters for identification and discrimination between the studied taxa. The different micro-morphological characters are presented in Table 2 and Figures 4-6. The epidermal cell wall is straight in two taxa and sinuous in three taxa. Stomata leveling are recorded in three types: superficial, in C. intybus var. foliosum and C. endivia subsp. pumilum, semi-depressed, in C. endivia var. endivia and C. endivia var. crispum, and depressed, in C. intybus var. intybus ( Figure 4).   Stephanocytic stomata: (1) Present. (2) Absent.

Morphological Identification
The data recorded in Tables 1 and 2 were applied to create the following bracketed key for the five taxa of Cichorium, which can help confirm their identity.

Trichomes
The following trichomes have been found on the leaves of the studied species: A.

Genetic Characterization and Polymorphism
The three studied PCR-based markers, RAPD, ISSR, and SCoT, demonstrated high and significant polymorphism and determined the taxon relationship ( Figure 7). Table 3 presents total, monomorphic, polymorphic, and unique bands, along with the percent of polymorphism calculated. The thirty primers revealed a total of 186 bands with an average of 6 bands per primer. The polymorphism summed up an average of 58%. A wide range has revealed polymorphism among three markers, as the following of 46% for ISSR, 62% for RAPD, 66% for SCoT-PCR. Primers OPA18 and SCoT-04 generated the highest polymorphism of 100%, while HB-12, SCoT-13, and SCoT-14 produced 25%, 16.7%, and 0%, respectively. Unique bands summed up 17 amplicons of which 5 bands are by RAPD, 7 bands by ISSR, and 5 bands by SCoT marker. The marker UBC807 recorded the highest number of unique bands (three bands). This variability can be used to differentiate the studied taxa.

Morphological and Genetical Relationship and Correlation among Cichorium Taxa
The morphological characters were analyzed numerically using the clustering method for identification and differentiation between them, a dendrogram using the UPGMA cluster analysis, is presented in Figure 8. The cluster analysis showed that species were grouped into two major clusters. Cluster I consisted of two taxa Cichorium intybus var.
Plants 2023, 12, 388 12 of 22 The morphological characters were analyzed numerically using the clustering method for identification and differentiation between them, a dendrogram using the UP-GMA cluster analysis, is presented in Figure 8. The cluster analysis showed that species were grouped into two major clusters. Cluster I consisted of two taxa Cichorium intybus var. intybus and Cichorium intybus var. foliosum. Cluster II comprised three taxa Cichorium endivia subsp. pumilum, Cichorium endivia var. crispum, and Cichorium endivia var. endivia. Genetic similarity was built as a dendrogram following Nei and Li coefficient using the UPGMA cluster analysis (Figure 9). The taxa are divided into two main groups, except the ISSR markers, which reveal a different result among taxa. The C. endivia var. crispum and C. endivia subsp. pumilum fell into the group, while C. intybus var. intybus and C. intybus var. foliosum fell into subgroup. The ISSR investigation showed similarity between C. intybus var. foliosum and C. endivia var. endivia, categorizing them into a single subgroup.  Genetic similarity was built as a dendrogram following Nei and Li coefficient using the UPGMA cluster analysis (Figure 9). The taxa are divided into two main groups, except the ISSR markers, which reveal a different result among taxa. The C. endivia var. crispum and C. endivia subsp. pumilum fell into the group, while C. intybus var. intybus and C. intybus var. foliosum fell into subgroup. The ISSR investigation showed similarity between C. intybus var. foliosum and C. endivia var. endivia, categorizing them into a single subgroup.
The dataset was investigated using clustering analysis to identify and differentiate the taxa. The cluster analysis ( Figure 10) showed that species were categorized into two major clusters, and Cluster II was further split into two groups. The first one consisted of two taxa-C. intybus var. intybus and C. intybus var. foliosum. Cluster II comprised three taxa and was further divided into two groups: Group 1 contained one taxon C. endivia var. endivia, while Group 2 had two taxa-C. endivia subsp. pumilum and C. endivia var. crispum.
Notably, the derived results are linked to those presented by morphological attributes. It seems likely that there is a significant correlation between C. endivia subsp. pumilum and C. endivia var. crispum and between C. intybus var. intybus and C. intybus var. foliosum. This may be due to the structure of taxon's genotype or the effect of evolution naturally.
Genetic similarity was built as a dendrogram following Nei and Li coefficient using the UPGMA cluster analysis (Figure 9). The taxa are divided into two main groups, except the ISSR markers, which reveal a different result among taxa. The C. endivia var. crispum and C. endivia subsp. pumilum fell into the group, while C. intybus var. intybus and C. intybus var. foliosum fell into subgroup. The ISSR investigation showed similarity between C. intybus var. foliosum and C. endivia var. endivia, categorizing them into a single subgroup.  Figure 9. Dendrograms classified the five taxa of Cichorium by three molecular markers using UP-GMA analysis.
The dataset was investigated using clustering analysis to identify and differentiate the taxa. The cluster analysis ( Figure 10) showed that species were categorized into two major clusters, and Cluster II was further split into two groups. The first one consisted of two taxa-C. intybus var. intybus and C. intybus var. foliosum. Cluster II comprised three taxa and was further divided into two groups: Group 1 contained one taxon C. endivia var. endivia, while Group 2 had two taxa-C. endivia subsp. pumilum and C. endivia var. crispum.
Notably, the derived results are linked to those presented by morphological attributes. It seems likely that there is a significant correlation between C. endivia subsp. pumilum and C. endivia var. crispum and between C. intybus var. intybus and C. intybus var. foliosum. This may be due to the structure of taxon's genotype or the effect of evolution naturally.  taxa and was further divided into two groups: Group 1 contained one taxon C. endivia var. endivia, while Group 2 had two taxa-C. endivia subsp. pumilum and C. endivia var. crispum.
Notably, the derived results are linked to those presented by morphological attributes. It seems likely that there is a significant correlation between C. endivia subsp. pumilum and C. endivia var. crispum and between C. intybus var. intybus and C. intybus var. foliosum. This may be due to the structure of taxon's genotype or the effect of evolution naturally. Figure 10. Dendrogram of the relationships between the five taxa of Cichorium based on the combined morphological and molecular characters using UPGMA analysis.
The correlation matrices possessed a broad sense of similarity ( Table 4). The lowest similarity was between the taxon 1 (C. intybus var. intybus) and 4 (C. endivia var. crispum)

Molecular Distance and Variance Decomposition
The distance to centroids (Table 5) and the variance decomposition (Table 6) of taxa's classes accounted more in the classification. All taxa were grouped into three classes, as in Figure 8. All markers revealed that C. intybus var. intybus and C. intybus var. foliosum dropped into class (I), C. endivia var. endivia categorized into class (II) only, and the C. endivia var crispum and C. endivia subsp. pumilum formed in class (III); except that the ISSR results showed a different pattern. The ISSR showed that the first class (class I) has C. intybus var. intybus only, the second (class II) has C. intybus var. foliosum and C. endivia var. endivia, and the third class (class II) includes the rest. The variance within the first class was 17.5, and the distance to centroids was 2.96 between C. intybus var. intybus and C. intybus var. foliosum, while the third class recorded a variance of 21.00, and the distance to the centroids was 3.24 between C. endivia var crispum and C. endivia subsp. pumilum. The second class, between C. intybus var. foliosum and C. endivia var. endivia, coming from ISSR showed an average variance of 3.50 and a distance to the centroids of 1.32, whereas the third class recorded an average variance of 5.50 and a distance of 1.66. The variance decomposition within and between classes for the optimal classification through three markers, is given in Table 5, the variance averaged 69% within the class, and 31% between classes for the combined markers. Markers showed that the variance within class recorded 60%, 63%, and 66% for RAPD, ISSR, and SCoT, respectively; whereas the variance between classes was 34.43%, 36.62%, and 40.34% for SCoT, ISSR, and RAPD, respectively.

Discussion
The morphological characteristics studied in this research, such as cypsela and pappus, using scanning electron micrographs, have already provided valuable information for specific genera [41,42]. The five taxa of Cichorium showed morphological differences. Identification and classification between taxa depend mostly on morphological characteristics. The studied taxa have a wide range of variations in characteristics associated with leaves (shape, type, texture, margin, and apex), cypselae (shape, color, and surface pattern), and trichomes (glands). Cichorium intybus is characterized by a spathulate leaf shape, a cypsela sulcate papillate surface pattern, a raised anticlinal wall, a concave periclinal wall, and a pappus type with scabrous scales. Cichorium endivia is characterized by having a leaf shape, simple or pinnately lobed, a slightly raised anticlinal wall, a slightly concave periclinal wall, and a pappus type with paleaceous scales to form a crown. The examined

Discussion
The morphological characteristics studied in this research, such as cypsela and pappus, using scanning electron micrographs, have already provided valuable information for specific genera [41,42]. The five taxa of Cichorium showed morphological differences. Identification and classification between taxa depend mostly on morphological characteristics. The studied taxa have a wide range of variations in characteristics associated with leaves (shape, type, texture, margin, and apex), cypselae (shape, color, and surface pattern), and trichomes (glands). Cichorium intybus is characterized by a spathulate leaf shape, a cypsela sulcate papillate surface pattern, a raised anticlinal wall, a concave periclinal wall, and a pappus type with scabrous scales. Cichorium endivia is characterized by having a leaf shape, simple or pinnately lobed, a slightly raised anticlinal wall, a slightly concave periclinal wall, and a pappus type with paleaceous scales to form a crown. The examined taxa demonstrated variations in their morphological features, such as leaf morphology, cypsela, and trichome characteristics. The five taxa had stomata on both surfaces, particularly the abaxial epidermis. Although they are very similar due to their morphological characteristics, C. intybus and C. endivia have always been categorized into two different species, morphologically described by Kiers et al. [43]. Kiers et al. [7] described C. intybus and C. endivia, the two cultivated and most known species, using an integration of morphological features with molecular approaches. Our results are in agreement with the view of Kiers et al. [7,43] and Raulier et al. [12].
Genetic identification of Cichorium using PCR-based molecular markers (RAPD, ISSR, and SCoT) enabled the detection of polymorphism to reveal the relationships between the studied taxa. Genetic analysis is crucial for managing the entire classification and identification, as well as genetic improvement [44]. The efficiency of a marker for discriminating species depends mainly upon the resultant polymorphism [22,24,45]. Markers of ISSR and SCoT have the potential to reveal polymorphism and offer a higher capacity for the determination of intra-and inter-genomic variations than other arbitrary primers such as RAPDs [21,26,46]. The difference in resolution resulting from RAPDs and ISSRs can be explained by the fact that different positions of the genome are targeted by the two-marker techniques [21]. Therefore, the ability to reveal genetic variability among and within species is directly related to the detected percentage of polymorphism using each marker than the technique employed. Similar conclusions were obtained by Mahdy [26] on lettuce and Jew's mallow and Gupta et al. [46] on Jatropha. Kiers et al. [7] studied endive and chicory cultivars using diagnostic AFLP markers in Cichorium species. Our results are in general agreement with several previous studies [28][29][30][31].
Dendrograms, as illustrated in Figures 8-10, have shown a correspondence between molecular markers and morphological attributes. The differences among the dendrograms generated by markers could be partially explained by the different number of PCR products analyzed, as presented in Table 6. This highlights the importance of higher genome coverage and loci number in estimating the genetic relationships among the tested taxa. Loarce et al. [47] obtained similar findings in barley. This could also be explained by the low reproducibility of RAPD markers [48]. The differences in the clustering pattern of genotypes using RAPD and ISSR markers may be attributed to the differences in marker reproducibility and genome coverage among the two tested markers; this highlights the importance of loci number and their genome coverage in obtaining reliable assessments of genetic correlations among taxa [21,22,47]; this may be helpful in genetic diversity, classification, taxonomy, systematics, and evolutionary biology [1,49,50]. Our results showed that the genetic identification and classification depend mainly on the efficiency of a marker [26,51].
Markers had categorized by variance decomposition C. intybus var. intybus and C. intybus var. foliosum into a group and C. endivia var. crispum and C. endivia subsp. pumilum into a group except those revealed by ISSR showing C. intybus var. foliosum and C. endivia var. endivia into a group and C. endivia subsp. pumilum and C. endivia var. crispum into a group, as shown in Table 4. That may be due to the variance in the resolution of ISSRs and targeting different loci of the genome by these techniques [21,26,51]. Earlier microsatellite markers could not differentiate between the species [52]. Additionally, it may be due to the makeup of taxon's genotype or the effect of evolution naturally.
The DCCA analysis of morphological and molecular characteristics revealed that Cichorium intybus var. intybus is related to C. intybus var. foliosum, while C. endivia var. endivia is related to C. endivia var. crispum and C. endivia subsp. pumilum. These results are consistent with those of Kiers [11] and Kiers et al. [43]. In earlier publications, it has been argued that the Egyptian chicory was classified into C. intybus [38][39][40]. The integrated approaches supports a better authentication and verification of the species and taxa. According to the results of this research we argue that the Egyptian chicory is classified into C. endivia subsp. pumilum.

Plant Materials
Cypselae of Cichorium species were obtained from the collection maintained by Vegetable Production Research Department, Agricultural Research Center (ARC), Giza, Egypt. Five taxa of the genus Cichorium were used in this study. Seeds and herbarium specimens of Cichorium taxa, Cichorium intybus var. intybus, C. intybus var. foliosum, C. endivia var. endivia, C. endivia var. crispum, and C. endivia subsp. pumilum were identified under the authority of the Herbarium, Botany Dept., National Gene Bank (NGB), Agricultural Research Center (ARC), Giza, Egypt.

Germination
Light intensities at mid-canopy were kept at approximately 400 µmols m 2 s −1 in the growth chambers for germination. A photoperiod was adjusted at 16 h of light and 8 h of darkness using fluorescent and incandescent lights. A daytime temperature of 23 • C and a nighttime temperature of 18 • C were maintained using chart recorders. The relative humidity was maintained at approximately 50%. First, the seed surface was sterilized using a solution of 5% sodium hypochlorite for 10 min and rinsed several times with sterile distilled water. Next, 10 seeds of each taxon were replicated in fours on a blotter, to which 10 mL of the test solution was added. Seeds germinated in the growing media containing peat moss, sandy soil, and perlite (1:1:1) under growth chamber conditions. Outer leaves at the basal nodes were taken for macromorphological and micromorphological analysis. Cypselae and leaves of each Cichorium taxon were separately cut into small sections of 4-8 mm long. Glutaraldehyde solution (6%, pH 7.3) was used to fix the sections for 12 h [53]. These were then rinsed with a 0.05 M C 2 H 6 AsNaO 2 (sodium cacodylate) buffer (pH 7.5) and rinsed with distilled water. This was then dehydrated with gradual ethanol concentrations (10-100%) for 20 min for each concentration. A Hitachi HCP-2 critical point dryer was used to dry the samples, which were then mounted onto aluminum stubs with carbon-coated sputtering (Elko IB-3 Ion Coater). JEOL (JSM-6390 LV) SEM, Model JEOLJSM-5500 LV was used to examine the samples. As in SEM, both fixation and dehydration procedures were conducted using energy-dispersive X-ray spectroscopy (EDX). NORAN System SIX software (V.1.8) was used for photomicrographs digitally taken at the Electron Microscopy Unit at the National Research Centre, Dokki, Egypt. The terminology for the cypsela, abaxial epidermis, and stomata used in this study follows Barthlott [54], Garg and Sharma [55], Mukherjee and Nordenstam [56], and Dilcher [57]. In addition, all morphological characters regarding the leaf, cypsela, and trichomes were documented to create classical keys.

Light Microscopy
A piece of the middle part of the leaf (1 cm 2 ) from each plant was taken and dehydrated in a series of ethanol concentrations (50-100%). The specimens were then embedded in paraffin wax (m.p. 58-61 • C) by xylol (solvent), sectioned at 15 µm on a Jung PM 2045 rotary microtome, and mounted on glass slides with egg albumen (adhesive agent). The wax was dissolved in xylol, and the slides were stained using light green and safranin. Using Canada balsam (mounting agent), permanent slides were prepared [58,59]. A digital camera was used to capture the photomicrographs.

Morphology
Twenty eight traits are presented including thirteen attributes of leaves and fifteen attributes of cypsela; the traits were estimated from approximately ten healthy plants from each taxon and are presented according to the relevant terminology [60].

DNA Extraction
The gDNA extraction was performed by the manufacturer's instructions of Zymo extraction kit (Zymo Research, Inc., Irvine, CA, USA). The DNA purity and quantity were checked via nanodrop and then stored for PCR analysis. The integrity of gDNA was verified by agarose gel electrophoresis in a 1% agarose/1 × TAE gel containing 1 × Sybr ® Safe DNA gel stain (Life Technology, Carlsbad, CA, USA). The isolated genomic DNA samples were diluted to 10 ng/µL. Then, good-quality gDNA samples were used for PCR amplification.

PCR-Based Markers
Three PCR-based markers were used for providing more information on Cichorium's genetic relatedness which are random amplified polymorphic DNA (RAPD), Inter Simple Sequence Repeats (ISSR), and start codon target (SCoT), as given in Table 3. RAPD-PCR amplification was carried out with ten synthesized random 10-mer arbitrary primers (Operon Biotechnologies, Inc., Ebersberg, Germany). The procedure was done as detailed in Williams et al. [20] and Williams and St Clair [30] with minor modifications. The amplification by ISSR to detect polymorphisms among accession for both species was carried out as described by Yang and Park [61] with slight modifications. The procedure of SCoT was designed by describing of Collard and Mackill [62], which synthesized by Operon Biotechnologies, Inc., GmbH, (Cologne, Germany).
The PCR reactions were performed in a 25 µL reaction mixture that contained 25 ng of template DNA, 0.2 µM dNTPs, 1 µM of each tested primer, 1.5 mM MgCl 2 , 1× PCR buffer, and 1 U of Go-Taq Flexi polymerase. In the initial denaturation cycle, the PCR program was adjusted at 94 • C for 5 min, then followed by 35 cycles. Each cycle involved 94 • C for 1 min, varying annealing temperature for each primer (Table 3) for 1 min, then 72 • C for 90 s, and 72 • C for 7 min in the final step for extension. The PCR amplification reaction products (Amplicons) were resolved in 1.0-1.5% agarose gel that contained ethidium bromide (0.5 µg/mL) in 1× TBE as a running buffer. A 100 bp plus DNA Ladder was used as molecular size standards.
PCR products were run on agarose gel in 1% agarose × TAE gel containing 1 × Sybr ® Safe DNA gel stain (Life Technology, Carlsbad, CA, USA) at 100 V for 30 min. Gels were visualized and photographed with a Gel Doc TM XR+ System with Image Lab TM Software (Bio-Rad ® ). Amplicon banding profiles were scored as present (1) or absent (0) in a binary matrix based on standard markers using Alpha Ease FCTM (version 4.0.1) software.

Statistical Analysis
Similarity for a binary matrix was estimated according to the Jaccard coefficient [63]. The dendrogram generated the Un-weighted Pair Group Method algorithms with Arithmetic (UPGMA) averages according to Nei and Li [64] to determine the genetic relationship among taxa. In addition, a Detrended Canonical Correspondence Analysis (DCCA) was performed using CANOCO V. 4.5 and CanoDraw V. 4.1. The dataset was entered into SPSS (version 14.0), as well as the add-in packages of StatistiXL (Kovach Computing Service 2013, version 1.8: http://www.xlstat.com (last accessed on 7 February 2022) and GenAlEx Genetic Analysis (version 6.5) in Microsoft Excel [65,66].

Conclusions
The integration of various identification methods, including macro-and micro-morphological and molecular characterization, plays a chief role in the identification and authentication of plant genera, species, and taxa. Although measuring the variability of morphological attributes does not provide extensive information, it can still be helpful for breeding and improvement programs. This is especially important in changing climates, including the Mediterranean region. The existence of these distinct taxa and their phylogenetic relationships were assessed and confirmed in this study using the phenological, and molecular markers, and phylogenetic methodologies. The approaches used in this study proved that these tools are helpful for phylogenetic studies at the species level or higher taxonomic ranks in the genus Cichorium.
We report that the leaf shape and type, the cypsela anticlinal and periclinal walls, pappus bristles, the epidermal cell wall, and the stomatal type were the most critical characteristics in the construction of the dichotomous indented key for Cichorium taxa. PCR-based identification confirmed these results revealed through the phylogenic tree. We observe that the integration of phenological and genetic characterization is helpful in the authentication of Cichorium taxa. Further research could focus on intra-species variability, diversity, and genetic differences among individuals of the Cichorium taxa. Despite the success of the molecular marker approach, we recommend the use of supplemental techniques such as DNA barcoding for improved classification and identification, along with more core and base collections of the studied plant materials. Our observations suggest that these taxa have the potential to provide rich genetic resources for further research in genetic biodiversity, conservation, and plant breeding programs. The chicory genetic assembly among different countries in the Mediterranean region visibly diverges with a firm amount of gene flow. The PCR-based markers could be utilized for analyzing genetic relationships and taxonomies of Cichorium taxa. Finally, it could be concluded that the Egyptian chicory belongs to the C. endivia subsp. pumilum.