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Article

Diversity of Crithmum maritimum L. from Salento Coastal Area: A Suitable Species for Domestication

by
Rita Accogli
1,
Eliana Nutricati
1,*,
Luigi De Bellis
1,
Massimiliano Renna
2,
Andrea Luvisi
1 and
Carmine Negro
1
1
Department of Biological and Environmental Science and Technologies (DiSTeBA), University of Salento, Via Prov. le Lecce-Monteroni, 73100 Lecce, Italy
2
Department of Soil, Plant and Food Sciences, University of Bari Aldo Moro, Via Amendola 165/A, 70126 Bari, Italy
*
Author to whom correspondence should be addressed.
Horticulturae 2024, 10(1), 81; https://doi.org/10.3390/horticulturae10010081
Submission received: 6 December 2023 / Revised: 9 January 2024 / Accepted: 12 January 2024 / Published: 14 January 2024
(This article belongs to the Topic Mediterranean Biodiversity)
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Abstract

:
Crithmum maritimum L., known as sea fennel, is an aromatic halophyte typical of the cliffs and coastal areas of the Mediterranean Sea and Atlantic Ocean. Their phytochemicals have been of great interest in the food and pharmaceutical industry. In this work, we analyzed, by SPME/gas chromatography coupled with mass spectrometry, the chemical variability of C. maritimum accessions in terms of volatile organic compounds. C. maritimum seeds were collected from different coastal sites in Salento, Southern Apulia, Italy, and subsequently cultivated ex situ. Several volatile compounds produced by C. maritimum leaves were detected, and, among them, D-limonene was found to be emitted at high levels by plants of all accessions representing the main compound, while other monoterpenes were produced at low levels. Moreover, the phenylpropene volatiles dillapiol and apiol (designated together as (dill)apiol) were emitted at variable amounts with different accessions. The correlation among groups based on volatile compounds has been analyzed using hierarchical cluster analysis, which has revealed three main groups based on (dill)apiol presence and its total amount in the cultivated plants of different geographic origins, confirming intraspecies biodiversity. Moreover, we have evaluated the seed germination and seedling development of C. maritimum in controlled conditions. We found no dormancy and a high germination rate for all samples analyzed. The chemo-diversity evidenced in cultivated plants obtained from seeds collected at different locations on the Salento peninsula is probably related to variations in climate resulting from different exposures along the coast. These findings highlighted the importance of C. maritimum as a suitable candidate for cultivation because it can tolerate harsh conditions/stresses and also has a possible use besides food and pharmaceuticals and for the restoration of coastal environments.

1. Introduction

Wild halophytes have been traditionally used since ancient times in different areas. In recent years, growing interest in the use of these plants has derived from the identification of many metabolites with health and nutritional properties. Recently, several studies dealt with the biology and origins of “sea fennel” or “rock samphire” Crithmum maritimum, their cultivation, chemical composition, and “omic” analyses showing their abundant contents, including beneficial nutrients for human health [1]. Traditionally, it has been included, in addition to several wild vegetables, in the Mediterranean diet, as reported by ethnobotanical studies [2]. Over the centuries, the use of the plant has decreased, but in recent years, more studies have highlighted its importance as an “emerging vegetable crop” [3].
Sea fennel, belonging to the Apiacae family represents a perennial facultative halophyte, growing in rocky sea cliffs, rarely in sands and gravel; it has a very wide distribution, occurring along the European Atlantic coasts, the Mediterranean and Black Sea coast, and Northwest Africa, where the plants are exposed to several abiotic stress, such as fluctuating soil salinity and drought [4]. C. maritimum developed morphological, physiological, and biochemical adaptations to tolerate salt excess; therefore, it was proposed as a potential crop for sustainable agriculture requiring few inputs as a “cash crop” [1]. Although it is able to survive in saline environments, its optimum growth occurs in salt-free or low-salinity grounds [5]. The aerial parts, rich in mineral elements, possess high nutritional values [6]; in addition, the species is employed in the food and pharmaceutical industries because of its high antioxidant power [7]. The phytochemical composition of aerial parts is variable depending on geographic distribution [8] and can be influenced by different abiotic stresses [9]. Chemical compositions are additionally influenced by different factors besides genotype, i.e., variable environmental factors [10].
The wide utilization of this species in several fields (medicine, food, agriculture, and environment) comes from the presence of several mineral elements, bioactive compounds, polyphenols, fatty acids, and flavonoids. Moreover, the ability to overcome water, salinity, and temperature stresses makes it suitable for growing in marginal lands and unproductive for traditional agronomic crops and in degraded coastal habitats [11]. Essential oils, widely used, release numerous volatile organic compounds (VOCs), including a large variety of chemical compounds classified as secondary metabolites.
Different factors, such as genetics (species, subspecies, and even varieties), physiological (development stage, organs), drying [12,13], storage, and even the method of volatile matter isolation, can significantly influence VOC profiles [14]. Nevertheless, VOC profiles in plants were strongly influenced by the environment [15]; therefore, the interaction between climate and genotype can affect the essential oil quality and yield [16].
Quantifying the metabolic diversity in plant populations is crucial for the efficient selection of plants for domestication programs. It is interesting to identify promising species with high adaptability capacity in the Mediterranean area, characterized by negative effects on agriculture due to climate change, including drought, soil erosion, desertification, and loss of biodiversity [17].
In the last decade, the increasing demand for sea fennel phytochemicals for industrial purposes has led to the development of efficient cultivation methods [18].
Based on these assumptions, we tested the seed’s germination and cultivation outside the natural environment of C. maritimum, employing seeds harvested from different sites along the Salento coasts, Apulia region, Italy. Moreover, we analyzed the VOC profiles of plants produced from the same seeds and grown ex situ under the same conditions to explore the chemical variability of C. maritimum accessions.

2. Materials and Methods

2.1. Plant Material and Experimental Conditions

Crithmum maritimum L. seeds were harvested in autumn 2022 from plants growing in six different localities of Salento area, Puglia, selected for different growth environments (Figure 1). Salento’s climate is typically windy and Mediterranean, with alternating mild winters, hot springs, torrid summers, and warm autumns; with regard to winds, the Salento peninsula is exposed to the Mistral and Tramontana (cool, dry winds) to the east, while on the Ionian side, to the west, it is exposed to the Scirocco (hot, humid wind). Rainfall is almost always below 500–700 mm. For each site, some climate data and the geographical coordinates, recorded with a GPS device, are reported in Table S1. A voucher (003/12/2022/halophyte) of samples analyzed was deposited in the Database of Botanical Garden, University of Salento, Lecce. The seeds were germinated in a greenhouse located in the Botanical Garden of the University of Salento. The seedlings were produced in polystyrene plug trays (cells with a diameter of 2.5 cm and volume of 21 mL) filled with peat. After growing in plug trays for 45 days, seedlings were transferred to 10 cm diameter plastic containers (0.5 L). A mixture composed of a peat-based substrate (Brill® 3, Brill Substrate GmbH & Co., Georgsdorf, Germany) and perlite (Agrilit 3, Perlite Italiana, Corsico-Milano, Italy), in a 2:1 (v/v) ratio, was used as growing substrate. The pots were placed on benches and grown using an ebb-and-flow hydroponic system. Plants were grown for 75 days with nutrient solution (NS) prepared with pre-collected raining water and containing (mg L−1) 119 nitrogen, 117 potassium, 16 phosphorus, 24 magnesium, 116 calcium, 54 sulfur, 1.12 iron, 0.27 manganese, 0.13 zinc, 0.27 boron, 0.03 copper, and 0.01 molybdenum, resulting in electrical conductivity of 1.8 dS m−1, pH 6.3; NO3-N:NH4-N at a percentage ratio of 84:16 was used as the nitrogen source. The experiment was organized in a fully randomized design with three replications for each geographic site, with every replica consisting of nine pots.
For the analysis of volatile compounds, the apical leaves of 6 cultivated plants were collected in July 2023 and processed as described below.

2.2. Germination Rate

Seed germination was measured by evaluating emergence of the radicle [19]. Five days after harvesting, the seeds were selected and purified by washing with sodium hypochlorite solution and then rinsed three times with demineralized water. For each sample, four replicates of 30 seeds were sown in Petri dishes containing filter paper soaked with demineralized water. The plates were placed in a phytotron at 25 °C with a photoperiod of 16 h light (light intensity of 10 kLx) and 8 h dark. Every day, the seeds with a protruding radicle were counted and removed from the dish. About three weeks after sowing time, the course and germination rate were evaluated. The germination parameter was determined for each seed accession and was expressed as mean of the 4 replicates with standard error. In Figure 2, the procedure for germination of C. maritimum seeds and ex situ cultivation was schematized.

2.3. Analysis of the Volatile Compounds

The analyses were carried out by solid-phase microextraction (SPME) methodology, as described previously by Negro et al. [20] and Dimita et al. [21]; the apical leaves of Crithmum plants, produced from seeds collected in the six different locations and grown in pots, were collected (1 g of fresh weight) and immediately sealed into 20 mL SPME vials (Agilent Technologies, Palo Alto, CA, USA) by metal screw-caps with pre-notched, Teflon-silicone septa, which is used for trapping the volatile organic compounds. The vials were then placed at 40 °C for 10 min in a thermostatically controlled bath to allow the evaporation of the compounds; hereafter, a SPME syringe was inserted, and the fiber (50/30 μm Divinyl-benzene/Carboxen/Polydimethylsiloxane, Supelco/Merck KGaA, Darmstadt, Germany), which was previously conditioned for 5 min at 235 °C in the gas-chromatograph injector, was exposed for 10 min to absorb the volatile compounds. Subsequently, the fiber was inserted into the injector port of gas chromatography with a mass-spectrometry detector (Agilent 7890B coupled with MS single quadrupole Agilent 5977A), and the desorption of the volatile compounds was performed at 235 °C for 4 min. At this point, the chromatographic run was started with an Agilent HP-5 MS column (30 m × 0.25 mm, 0.25 μm) (where temperature was raised from 60 °C to 230 °C, with a constant increase of 3 °C/min), with a helium (purity > 99.999%) constant flow of 1.0 mL/min. Compounds were identified by library search and analytical standards if available. The mass spectrum of an unknown compound was searched in a data-processing system. Substances with a score above 800, both for identity and purity, were putatively identified after comparing the detected compound with the one in the NIST Computational Chemistry Comparison and Benchmark database. Retention index (RI) was obtained, as reported by Zhao et al. [22], being employed as a reference of the retention times of a series of C8–C20 alkanes separated under the GC-MS conditions mentioned above.
All the statistical analyses described were carried out using the percent content value of each compound on the total VOCs, considering the mean value of the three technical replicates for each compound.

2.4. Agglomerative Hierarchical Cluster (AHC) Analysis of Volatile Organic Compounds

Data preprocessing and statistical analyses were conducted using XLSTAT for Windows (Version 2021.3.1). Metabolite concentration data were imported, and an agglomerative hierarchical clustering analysis was performed, utilizing Ward’s minimum variance method to determine the clusters. The dendrogram representation of the clusters was generated, providing a visual summary of the similarity (Euclidean distance) between the metabolite profiles from the six different locations.

3. Results

3.1. Seed Germination

The germination rates of seeds collected from six different sites along the Salento coast are shown in Figure 3. Germination was completed in approximately three weeks, and no dormancy was observed; the lowest germination was recorded for seeds collected in Gallipoli, but the value remained above 50%, while those from Tricase, Otranto, and Torre Lapillo showed the highest germination values (above 80%); finally, the seeds from Santa Maria di Leuca and San Cataldo showed slightly lower germination rates, about 79% and 78%, respectively.

3.2. Volatile Organic Compounds

The GC-MS analysis of sea fennel leaf VOCs highlighted different chromatographic profiles among different C. maritimum accessions grown in a greenhouse, allowing us to identify more than 25 volatile organic compounds (Figure 4).
The peak area values (%) of the identified volatile compounds are reported in Table 1. The predominant compound was D-limonene, which is present at a high level in all chromatograms, up to a value of about 92% for the Tricase accession. The content of monoterpenes cis/trans β-Ocimene and β-Mircene was low in all samples; the amount of phenylpropanoids dillapiol (4,5-dimethoxy-6-prop-2-enyl-1,3-benzodioxole) and apiol (4,7-dimethoxy-5-prop-2-enyl-1,3-benzodioxole), both indicated as (dill)apiol because our chromatographic system did not allow us to distinguish between the two compounds (having just a methoxy group positioned differently on the benzene ring), was high for the San Cataldo accession (about 34%), and Gallipoli and Torre Lapillo accessions showed an amount of about 20% and 12%, respectively. These compounds were detected at the lowest levels in samples from Otranto and S. Maria di Leuca and undetected for Tricase.
The γ-terpinene was observed in samples collected from San Cataldo and Torre Lapillo, and sabinene was found to be emitted only from the leaves of S. Maria di Leuca accession.
A compound found at a low level only in plants from San Cataldo was Panaxynone, a polyacetylene also known as Falcarinone, with a level of about 4%.

Agglomerative Hierarchical Cluster Analysis on VOC Composition

A hierarchical cluster analysis (HCA) was performed for the evaluation of the volatile fingerprints of C. maritimum from different sites and to evaluate the chromatographic differences in the volatile compound contents. Ward’s algorithm was employed in the analysis. Clusters and sub-clusters are visualized in a dendrogram plot (Figure 5). As shown in Figure 5, two well-separated clusters are visualized: a cluster was represented by plants from San Cataldo, which were distinguished from other Crithmum groups for high (dill)apiol content (>30%), the second cluster, characterized by a lower (dill)apiol amount, grouped the other five accessions/sites analyzed. Moreover, this cluster was divided into two subclusters: one comprises Gallipoli and Torre Lapillo accessions with a (dill)apiol content between 10 and 30%, and the other Tricase, Otranto, and S. Maria di Leuca groups, with phenylpropanoid amounts of <10%.

4. Discussion

Given the interest in the exploitation of C. maritimum to enhance the production ex situ, we evaluated the germination efficiency. Our results showed that the seeds have a high germination rate (average value of about 78%) and no significant dormancy in controlled conditions, suggesting a great potential for introduction in culture despite the reported need for improved germination for C. maritimum cultivation [23]. A similar level of germination was obtained by Nimac et al. [24]. However, differences in germination between seeds collected from different sites (Figure 3) suggest intraspecific variability in germination patterns reported for other species [25,26] and for C. maritimum seeds from Italy or from the England Atlantic coast [27]. These results highlight an important trait for the Salento accessions that should help C. maritimum cultivation on a large scale.
Comprehensive information about the presence of different metabolites could represent a prerequisite to investigating the biodiversity of organisms belonging to the same species to develop domestication programs. In this study, the different composition of VOCs produced by C. maritimum plants obtained from seeds collected in six sites along Salento coasts was evaluated. Through gas chromatography, 25 volatile chemical compounds were identified; most of them are monoterpenes (Table 1), sesquiterpenes, and phenylpropanoids, such as (dill)apiol. We observed quantitative and qualitative differences in the mix of volatiles released from distinct plant accessions.
Terpenoid VOCs play an important role in direct and indirect plant defense [28]. In recent years, many studies reported that sea fennel contains a wide variety of chemical constituents, such as phenolic compounds [29], and volatile compounds, such as limonene, α-pinene, p-cimene, γ-terpinene, and β-myrcene, have been found in essential oils from different plant portions [30,31].
In this work, data obtained by the GC analysis of VOCs emitted by the apical leaves of plants grown in a greenhouse (within the Botanical Garden of the University of Salento) show a common feature in D-limonene as the most abundant compounds: more than 60% in Otranto, Tricase, S. Maria di Leuca, and Gallipoli accessions, nearly 50% for Torre Lapillo samples, and about 38% for plants from San Cataldo. In wild plants growing in Central Italy and in Sicily, limonene represents a major essential oil component [8,32], suggesting that Crithmum plants growing in Italy belong to a chemotype characterized mainly by this monoterpene. Similarly, a great amount of D-limonene was found in essential oils from Turkey [33] and Croatia [34] plants.
Data obtained from AHC analysis highlighted that there are two main clusters, probably related to different chemotypes: one named, according to the review of Renna [3], the phenylpropanoid-type, typical of the San Cataldo site, which has, in addition to monoterpenes, a high level of (dill)apiol, and the other, namely monoterpene hydrocarbon-type, characterized by the prevalence of different combinations of D-limonene, c/t β-Ocymene, β-mircene, γ-terpinene, and several cyclic monoterpenes at low concentrations.
However, the high variability in the phenylpropanoid content observed in the six accessions (Table 1) led us to focus on two subclusters obtained from AHC analysis, one related to Gallipoli and Torre Lapillo samples, showing a (dill)apiol amount between 10 and 20%, the other including Tricase, Otranto, and S. Maria di Leuca samples, represented by plants with a (dill)apiol concentration less than 10%. Therefore, we assume the presence of three probable chemotypes: the first, named chemotype I (high (dill)apiol), represented by San Cataldo accession, characterized by a (dill)apiol content > 30%; the second one, named chemotype II (medium (dill)apiol), with a (dill)apiol content between 10 and 20%, including Gallipoli and Torre Lapillo accessions; and the third, named chemotype III (low (dill)apiol), for Otranto, S. Maria di Leuca, and Tricase accessions with a (dill)apiol amount < 10%. An interesting finding from the data is that (dill)apiol has not been detected in the Tricase samples.
In a study carried out to characterize the chemical composition of a Portuguese C. maritimum essential oil, Pateira et al. [35] identified two chemotypes based on the dillapiol amount in extract: chemotype 1 with dillapiol > 14.5% and chemotype 2 with dillapiol < 5.8%. Numerous Apiacae species were characterized by a high content of volatile phenylpropanoids as (dill)apiol [36]. In Piper lanceaefolium, different chemotypes were identified based on the (dill)apiol content [37].
The comparison of the chemical composition of C. maritimum plants from Apulia with other Italian regions evidenced that a phenylpropanoid-type chemotype of Crithmum, characterized by a significant amount of dillapiol, obtained by the hydrodistillation method, was found only in Sardinia [38].
Due to the presence of several monoterpene compounds in all samples, we compared our data with those from previous studies about essential oil characterization in C. maritimum with different geographic origins, such as Cyprus [39], France [8], Spain [40], Turkey [33], and Greece [18,41]. In agreement with our findings, some authors have found that the most abundant volatile compounds identified in C. maritimum leaves were terpenoids with different combinations of essential oils [42,43].
An interesting finding in the data is that, among terpenoid compounds, we detected a significant amount of sabinene, a cyclic monoterpene, for Maria di Leuca accession, while only traces were detected for Tricase accession. These data, together with the absence of (dill)apiol, could explain why, in cluster analysis (Figure 5), the Tricase sample diverged from Otranto and S. Maria di Leuca. A combination of sabinene and limonene as the major compounds in S. Maria di Leuca was a common trait with the essential oil extracts from plants growing in Dalmatia (Croatia) [34].
Moreover, the evaluation of all compounds identified in Table 1 showed an important variation in the minor compounds, which contribute together with different combinations of major compounds to the determination of intraspecific variability. It is likely that, over time, varying soil and environmental conditions have influenced the chemical composition of the chemotypes highlighted, although grown in a small area like Salento.
A result worth noting is that in plants from San Cataldo, we detected panaxynone (also known as falcarinone), a polyacetylene previously isolated from almost all species belonging to several families, including Apiaceae. This is the first time that it was identified in C. maritimum. Previous studies reported the identification in Panax ginseng and Dacus carota roots [44,45]; Meot-Duros et al. [9] highlighted the presence of falcarindiol in C. maritimum plants from Britanny. Falcarinone, together with falcarinol and falcarindiol, belongs to highly bioactive compounds with cytotoxic, anti-inflammatory, and potential anticancer properties [46].
Among the compouns identified in the plants of Salento, it is interesting that some of them determine aromatic characteristics, which are employed, adding to food or cosmetic products. D-limonene, found in all Apulian accessions, occurring more commonly in nature as the fragrance of oranges, is a flavoring agent in food manufacturing and some medicines; it is also used as a botanical insecticide [47,48].
γ-terpinene has strong antioxidant activity, has a wood/lemon/lime odor, and is widely used in the food, flavor, soap, cosmetic, pharmaceutical, and perfume industries [49]. The spicy sabinene contributes to the savory flavor of black pepper and the earthy taste of carrots. It is popular in aromatherapy and is a major constituent of essential oils with therapeutic qualities, such as carrot seed oil and tea tree oil [50].
The phenylpropene volatiles dillapiol and apiol impart one of the characteristic aromas of dill (Anethum graveolens) weeds [51]. Dillapiol is a phenylpropanoid with one methylene-dioxy and two methoxy groups; in apiol, a methoxy group is positioned differently on the benzene ring. It is known that dillapiol showed insecticide activity inhibiting cytochrome P450 monooxygenases acting on insect metabolism, blocking the insect catabolism of xenobiotics as plant toxins [52,53]. Razzaghi-Abyaneh et al. [54] evidenced that dillapiol and apiol inhibit the ability of Aspergillus parasiticus to synthetize aflatoxins. Apiol has been demonstrated to inhibit human colon cancer cells [55].
β-ocimene, found in all accessions analyzed, belongs to acyclic monoterpenoids, and it has a citrus, green woody aroma along with a green floral or woody taste. It is an approved food additive and is used in perfumery products. Ocimene occurs naturally in several plants and fruits, including basil, coriander, mint, and mangos, and it is also a constituent of the pheromones of several insects [56]. It has many biological functions, such as its use in pesticides and as a defense against herbivores [57].
From a sensorial point of view, VOC analysis can explain some interesting attributes of C. maritimum, translating into some notes of celery, common fennel, and peel of green citrus with a pungent aftertaste [58].
Overall, the variability observed presents good practice to fulfill the demand of food and pharmaceutical industries. Therefore, different chemotypes of C. maritimum may be employed as needed in many fields, depending on the combination and amounts of VOCs.

5. Conclusions

The intraspecies diversity based on qualitative and quantitative metabolites is an efficacious approach to understanding the interaction plant environment, especially in wild plants, which have the ability to adapt to challenging climatic conditions. C. maritimum L. is considered an emerging crop for its physiological potentialities, high nutritional value, and biological effects. The high germination rate and the growth of seedlings in open fields suggest that C. maritimum could be cultivated in soils with non-agronomical importance to produce a source of high quality for industrial purposes.
As a result, we suggested that in Salento, there are three main C. maritimum chemotypes depending on (dill)apiol content, according to the clusters and subclusters obtained from AHC analysis: a chemotype I (high (dill)apiol) with a content > 30%, a chemotype II (medium (dill)apiol) between 10 and 30%, and a chemotype III (low (dill)apiol) < 10%.
Although we have considered three different chemotypes based on (dill)apiol content, we found a high diversity, in terms of terpenoids identified among the six C. maritimum accessions of plants, each characterized by a specific VOC composition.
Our findings provide a better understanding of the phytochemistry of this species useful for domestication programs and the commercial cultivation of aromatic plants. Further studies are needed (i) to deepen the chemical peculiarities of each accession through the analysis of essential oils in different organs during the life cycle and (ii) to evaluate the optimal conditions that have a high yield in terms of valuable metabolites.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/horticulturae10010081/s1, Table S1: GPS coordinates and characteristics of six sites of Salento, Apulia region in Italy, considered in this study; Figure S1: Time course of seed cumulative germination (%) rates of C. maritimum. The results are presented for plants from different sites. Each line represents a replicate of 100 non dormant seeds.

Author Contributions

Conceptualization, C.N., R.A. and L.D.B.; methodology, C.N. and R.A.; formal analysis, C.N. and E.N.; investigation, C.N., M.R. and R.A.; resources, R.A. and M.R.; data curation, C.N. and A.L.; writing—original draft preparation, E.N. and C.N.; writing—review and editing: E.N., C.N., M.R. and L.D.B.; supervision, A.L. and L.D.B.; funding acquisition, L.D.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Regione Puglia Administration under the Rural Development Program 2014–2020, Project ‘Biodiversity of Apulian vegetable species (BiodiverSO Veg)’, Measure 10, Sub measure 10.2, Operation 1 “Program for the conservation and the valorization of the genetic resources in agriculture” (DDS n. 04250182807, CUP: B97H22003760009)-n. 7.

Data Availability Statement

Data are contained within the article.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Geographical location of Apulia and Salento in relation to the Italian peninsula and indication of the places (red arrows) along the Salento coast where the seeds of the different C. maritimum accessions were collected.
Figure 1. Geographical location of Apulia and Salento in relation to the Italian peninsula and indication of the places (red arrows) along the Salento coast where the seeds of the different C. maritimum accessions were collected.
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Figure 2. Scheme of procedures for seed germination and ex situ cultivation of C. maritimum.
Figure 2. Scheme of procedures for seed germination and ex situ cultivation of C. maritimum.
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Figure 3. Germination rates of seeds of six different C. maritimum accessions of Salento coast. Bars indicate standard error.
Figure 3. Germination rates of seeds of six different C. maritimum accessions of Salento coast. Bars indicate standard error.
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Figure 4. Representative chromatograms showing the main VOCs emitted by aerial parts of C. maritimum from six sites analyzed, San Cataldo Otranto, Tricase, S. Maria di Leuca, Gallipoli, Torre Lapillo. The numbers refer to the most significant compounds. The peak identified with n. 10 is out of scale.
Figure 4. Representative chromatograms showing the main VOCs emitted by aerial parts of C. maritimum from six sites analyzed, San Cataldo Otranto, Tricase, S. Maria di Leuca, Gallipoli, Torre Lapillo. The numbers refer to the most significant compounds. The peak identified with n. 10 is out of scale.
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Figure 5. Dendrogram of agglomerative hierarchical cluster analysis of C. maritimum from six sites in Salento coastal area with remarks on the volatile organic compounds.
Figure 5. Dendrogram of agglomerative hierarchical cluster analysis of C. maritimum from six sites in Salento coastal area with remarks on the volatile organic compounds.
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Table 1. Main VOCs emitted by C. maritimum leaves from six different accessions (San Cataldo, Otranto, Tricase, S. Maria di Leuca, Gallipoli, and Torre Lapillo) in Salento coast. Numbering of volatile compounds respects the order of elution after the analysis of aerial parts of plants. Major compounds are those with a peak area of >4% of the total.
Table 1. Main VOCs emitted by C. maritimum leaves from six different accessions (San Cataldo, Otranto, Tricase, S. Maria di Leuca, Gallipoli, and Torre Lapillo) in Salento coast. Numbering of volatile compounds respects the order of elution after the analysis of aerial parts of plants. Major compounds are those with a peak area of >4% of the total.
No.Compound NamePeak Area (%)RIaRIb
San CataldoOtrantoTricaseS. Maria di LeucaGallipoliTorre Lapillo
1Unknown 0.6 0.3960-
2Δ3-Carene0.4 2.61.5 9781005
3Cyclofenchene 1.2 3.54.1981946
4Sabinene 0.218.0 985978
5β-Phellandrene 3.90.410011004
6β-Pinene 0.1 1005990
7β-Myrcene0.71.21.81.91.71.71013992
8α-Terpinene 0.410211014
9Cymene 2.910241020
10D-Limonene37.876.392.064.766.449.310281031
11(c/t) β-Ocimene 5.05.62.43.1 1.010321032
12(c/t) β-Ocimene0.30.30.2 2.4 10341032
13γ-Terpinene13.3 0.8 27.910621064
14Allocimene 1.2 11221131
15α-Terpineol0.3 0.1 11821190
16α-Copaene0.3 13761376
17 β-Caryophyllene 0.3 14181417
18α-Bergamotene 0.2 1.2 0.4 14271438
19α-Cedrene 0.1 14331446
20 β-Bisabolene 0.1 14981505
21 β-Sesquiphellandrene 0.1 0.3 15221524
22 G ermacrene B 0.5 0.1 0.50.415561558
23(Dill)apiol 11.90.9 16781681
24(Dill)apiol 22.50.3 5.020.211.616811681
25Panaxynone4.2 20222018
Total compounds identified %97.287.310096,899,3100
Monoterpene hydrocarbons57.585.899.390.677.988
Oxygenated monoterpenes0.3 0.1
Sesquiterpenes hydrocarbons0.80.30.61.21.20.4
Phenylpropanoids34.41.2 5.020.211.6
The values given are the averages of three repetitions, and standard error values are not reported but were all values within 5%. RIa, Retention index calculated, RIb, Retention index data from the NIST library (https://webbook.nist.gov/chemistry/, accessed on 28 December 2023).
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Accogli, R.; Nutricati, E.; De Bellis, L.; Renna, M.; Luvisi, A.; Negro, C. Diversity of Crithmum maritimum L. from Salento Coastal Area: A Suitable Species for Domestication. Horticulturae 2024, 10, 81. https://doi.org/10.3390/horticulturae10010081

AMA Style

Accogli R, Nutricati E, De Bellis L, Renna M, Luvisi A, Negro C. Diversity of Crithmum maritimum L. from Salento Coastal Area: A Suitable Species for Domestication. Horticulturae. 2024; 10(1):81. https://doi.org/10.3390/horticulturae10010081

Chicago/Turabian Style

Accogli, Rita, Eliana Nutricati, Luigi De Bellis, Massimiliano Renna, Andrea Luvisi, and Carmine Negro. 2024. "Diversity of Crithmum maritimum L. from Salento Coastal Area: A Suitable Species for Domestication" Horticulturae 10, no. 1: 81. https://doi.org/10.3390/horticulturae10010081

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