Next Article in Journal
A GATA Transcription Factor from Soybean (Glycine max) Regulates Chlorophyll Biosynthesis and Suppresses Growth in the Transgenic Arabidopsis thaliana
Next Article in Special Issue
Document or Lose It—On the Importance of Information Management for Genetic Resources Conservation in Genebanks
Previous Article in Journal / Special Issue
The Cypriot Indigenous Grapevine Germplasm Is a Multi-Clonal Varietal Mixture
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Plants
Volume 9
Issue 8
10.3390/plants9081035
plants-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Genetic Distinctiveness Highlights the Conservation Value of a Sicilian Manna Ash Germplasm Collection Assigned to Fraxinus angustifolia (Oleaceae)

by
Loredana Abbate
1,†,
Francesco Mercati
1,*,†,
Giuseppe Di Noto
2,
Myriam Heuertz
3,
Francesco Carimi
1,
Sergio Fatta del Bosco
1 and
Rosario Schicchi
2
1
Institute of Biosciences and Bioresources (IBBR), National Research Council, Corso Calatafimi 414, 90129 Palermo, Italy
2
Department of Agricultural, Food and Forestry Sciences (SAAF), University of Palermo, Via Archirafi 38, 90123 Palermo, Italy
3
Institut National de Recherche Pour l’agriculture, l’alimentation et l’environnement (INRAE), Univ. Bordeaux, BIOGECO, 69 route d’Arcachon, F-33610 Cestas, France
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Plants 2020, 9(8), 1035; https://doi.org/10.3390/plants9081035
Submission received: 24 July 2020 / Revised: 10 August 2020 / Accepted: 12 August 2020 / Published: 14 August 2020
(This article belongs to the Special Issue Plant Biodiversity and Genetic Resources)
Browse Figures
Review Reports Versions Notes

Abstract

:
The cosmopolitan genus Fraxinus comprises about 40 species occupying several habitats in the Northern Hemisphere. With some species hybridizing and sharing genetic variants, questions remain on the species assignment of germplasm within the genus Fraxinus despite numerous species-specific assessments. A multidisciplinary approach was employed to provide a definitive insight into the genetics of an endangered Fraxinus “manna ash” collection, located in a rich plant biodiversity hotspot of the Madonie Mountains (Sicily). Although the collection size was small, genetic diversity, assessed by chloroplast (cpSSR) and nuclear (nSSR) microsatellites (SSR—Simple Sequence Repeats), allowed identifying three different chloroplast haplotypes, with one (H5) dominant, and several polymorphic loci, able to discriminate most of the local accessions studied. Molecular data were linked to cytofluorimetric and phenotypic evaluations and, contrary to popular belief that manna ash is Fraxinus ornus L., the germplasm currently used for manna production belongs to Fraxinus angustifolia Vahl. Interestingly, joint analysis of our genetic panel with a large European dataset of Fraxinus spp. suggested the presence of a possible glacial refuge in Sicily, confirming its importance as biodiversity source. Our results will be helpful for the design of long-term conservation programs for genetic resources, such as in situ and ex situ conservation, seed collection and tree reintroduction.

1. Introduction

The genus Fraxinus (Oleaceae) comprises 45–65 tree species and is represented across large areas of Europe, Asia and North America [1,2]. Fraxinus species show considerable variability in their flowering biology, ecological requirements and distribution ranges as a result of dispersal and vicariance processes as well as adaptive evolution underlying diversification in the genus [3].
In Europe, three ash species are present: the common ash, Fraxinus excelsior L., the flowering ash, Fraxinus ornus L., and the narrow-leaved ash, Fraxinus angustifolia Vahl [4]. F. excelsior, a polygamous species with male, female and hermaphrodite individuals, [5,6], is found throughout the continent except in the Mediterranean region, while F. ornus is androdiecious [3] and grows in relatively high altitude areas of the eastern Mediterranean basin [7,8]. Finally, F. angustifolia, a close relative to F. excelsior, shows hermaphrodite flowers and is very common around the Mediterranean basin and to the west of the Black Sea in the Danube basin. Due to the level of local adaptation [9], different botanical names were assigned to F. angustifolia. Three groups can be identified at subspecies level, structured by geographical regions [7,10]: F. angustifolia ssp. oxycarpa (Bieb. ex Willd.) Franco and Rocha Afonso observed in the in East Central and Southeastern Europe, including the Balkans; F. angustifolia ssp. syriaca (Boiss.) Yalt. in the east of Europe, from Turkey to Pakistan; and F. angustifolia ssp. angustifolia in southwestern Europe. While F. excelsior grows on a wide range of soil types, preferring nutrient-rich substrates, F. angustifolia grows near surface and ground waters, and thus its habitat is more restricted [11,12]. Indeed, the distribution of this species in the Mediterranean region is irregular and limited to smaller and isolated populations on drier sites at higher altitudes or on wetland sites [13]. The levels and distribution of genetic diversity in F. excelsior and F. angustifolia reflect the differential climatic and ecological affinities of both species, as well as the signature of ancient and contemporary hybridization [4,14].
Sicily boasts several botanical highlights. Both trees and endemic herbs survived through the last glacial maximum, highlighting the role of Sicily as a refuge area for thermophilous European plants during glacial times [15]. In addition Sicily, the biggest region of Italy, has been identified as one of 52 putative glacial refuges based on phylogeographic data from trees and herbs, and lies within one of ten regional hotspots of plant species biodiversity in the Mediterranean basin [16].
The presence of the genus Fraxinus in Sicily is restricted mainly to scattered groves and natural populations of F. angustifolia and F. ornus spread in the hilly area of the Madonie and Nebrodi Regional Natural Parks, at altitudes between 100 and 900 m a.s.l. In this area, the relevance of Fraxinus spp. is extremely high, from economical, botanical, naturalistic and historical points of view [17,18]. In fact, the F. ornus cultivation, brought to Sicily at the time of the Arab invasion (ninth-eleventh century) and known as manna ash, is grown for the production of manna, a crystal coagulate exuding after cutting 5–10 cm long slits with a billhook along and inside the whole thickness of the bark. From these slits a purplish and bitter liquid flows out. After contact with the air, this liquid turns white and becomes sweet, rapidly coagulating and forming crystal-like layers, called manna. Then manna is harvested and placed in specific trays for drying. Its production varies from 0.2 to 1.5 kg per tree per year, depending on ash cultivar [18]. However specific pedoclimatic conditions (persistent dry, hot periods and steady ventilation during summertime) are mandatory for the bioaccumulation of osmotic sugars in the phloem of Fraxinus and to obtain the complete drying of the sap that exudes from cuttings. The most abundant constituent of manna is mannitol (around 50% of total chemical compounds), a hexavalent alcohol known also as “manna sugar”; monosaccharide, oligosaccharide, mineral and volatile constituents are also well represented [18,19]. Due to its characteristics, the manna is used in cosmetic, pharmaceutical and confectionary industries [20]. In Sicily, the presence of Fraxinus groves has given rise to a traditional agroforestry landscape of unique value and relevant economic importance until the late 1950s. In the last 50–60 years, after the introduction of synthetic mannitol, the integrity and the extension of the manna ash landscapes have been dramatically reduced. Today, because of habitat fragmentation, naturally poor regeneration and land use change, the maintenance of the crop is threatened. The present landscape of Sicilian manna Fraxinus is limited to a fragmented and isolated area of few hundreds of hectares in the territory around Castelbuono and Pollina (Palermo-Italy), in which natural populations, single and scattered trees are distributed. Large differences in several phenotypic traits, such as leaf morphology, inflorescence features and infructescence characteristics, are observed among the different plants. However, based on their distinctive morphological features, several cultivars (or varieties) were distinguished and identified with dialect names, since the nineteenth century [17,20,21,22]. The declining status of the manna ash germplasm has been confirmed by the last survey on the residual consistency of the crop in the Madonie Mountains [17,18]. In less than 150 years, about 50% of the germplasm of the manna ash cultivars has been lost; therefore, both the germplasm of the cultivated varieties and the ash cultivation are threatened with extinction. Previous studies, based on morphological and chemical analysis, confirmed the presence of 16 cultivars, 13 of which putatively belonging to F. angustifolia and the remaining three putatively belonging to F. ornus [17]. However, the value of these approaches to characterize manna cultivars and varieties is limited due to their drawbacks, such as the influence of environment on trait expression, epistatic interactions and pleiotropic effects. Therefore, there is an urgent need to focus on the unknown genetic background, structure, relationships and diversity of the Fraxinus gene pool distributed in Sicily, to provide useful information aimed both to prevent biodiversity loss, safeguarding this endangered plant populations, and develop future breeding programs.
Microsatellite (SSR, simple sequence repeat) markers are codominant, highly polymorphic, reproducible, well distributed throughout the genome and suitable for automated analysis, and are; therefore, widely used markers for plant variety characterization [23,24,25,26,27,28]. SSRs have proved to be ideal tools, in conjunction with analysis of morphological characteristics, for analyzing genetic diversity and structure and evolutionary relationships between populations of rare, isolated and endangered species. Chloroplast DNA sequences are suitable tools to highlight the postglacial colonization routes [4,29,30] because they are usually non-recombinant in angiosperms and they are transmitted through seeds only [31,32], implying that the effective population size is more reduced for chloroplast DNA than for nuclear DNA. Nuclear and plastid DNA microsatellites have been extensively used to describe the phylogeography of Fraxinus spp. and clarify the hybridization process among ash species [4,14,33,34].
Nuclear DNA content has an important role in systematics, and it is a useful tool in biodiversity evaluation [35,36]. Flow cytometry is a quick and effective method to assess genome size (i.e., the amount of DNA in cell nuclei) [37,38]. Studies of genome size variation can shed light on the molecular mechanisms underlying this type of variation [39,40,41], which is a relevant indicator of genetic divergence and speciation processes [42,43].
In this study, we used morphological traits, genetic profiles (nuclear and plastid SSR markers) and genome size estimates (nuclear DNA content) to characterize the biodiversity within and among native accessions of Fraxinus in Sicily, belonging to a historical manna ash collection that, from previous studies [18], seems to be represented by varieties mainly characterized as F. angustifolia. We also present the first assessment of evolutionary relationships between the F. angustifolia germplasm from Sicily and F. angustifolia germplasm from throughout Europe. Knowledge of the extent of genetic diversity and characterization of population genetic structure of native Fraxinus spp. in Sicily will have important implications for the conservation of this biodiversity, to provide useful knowledge for the management of the manna ash germplasm collection, in-situ/ex-situ conservation and to save this precious cultural heritage.
This analysis is a first step towards selecting breeding material and establishing conservation strategies to sustain and potentially increase the overall production and productivity of manna ash and the continual use of this agroforestry tree resource through varietal improvement and suitable agronomic practices under southern Mediterranean conditions.

2. Materials and Methods

2.1. Plant Material

Leaf samples of native manna ash (Fraxinus spp.) germplasm located in Madonie National Park (Palermo, Sicily; 37°53′ N 14°01′ E/37.883° N 14.017° E) were collected. Individual trees were selected according to specific criteria based on morphological features, historical notes and their use for manna production [17,18,21,22,44]. The list of accessions studied, and their dialectical name, is indicated in Table 1 and Table S1. At least three individual trees (replicates) were collected for each local variety studied, except for monumental trees. In total thirty-four (34) trees (accessions) were analyzed. Four F. ornus trees, collected in the same area, were also added in the study and used as reference. Young and fully expanded leaves were immediately frozen in liquid nitrogen and conserved at −80 °C until used for DNA extraction. This sample set, comprising 38 accessions (Table S1) belonging to manna ash varieties and F. ornus (FOR) collected in Sicily, is named sample set #1 from here on.
To full investigate genetic relationships and population genetic structure among the analyzed manna ash accessions and natural populations of Fraxinus spp., our sample set (#1) was added to SSR profiles already available. To avoid redundancy in the results, this second sample set (#2) included only samples showing unique genetic profiles isolated from sample set #1, and SSR unique profiles of 475 individual ash trees described in Gérard et al. (2013) [14], belonging to F. angustifolia (148; FAN), F. excelsior (274; FEX) and hybrids between F. angustifolia and F. excelsior (53; HYB) collected in the natural, partially overlapping, distribution ranges of the two species across Europe (Table S2). This second sample set is named sample set #2 from here on.

2.2. Morphological Trait Variation

For each accession from set #1, including four F. ornus trees, a set of morphological traits were evaluated (Table S1). The most discriminant morphological features among Fraxinus species (e.g., the samara stalk length, the number of samaras/raceme, the colour of apical buds) were recorded; three replicates for each trait were evaluated.

2.3. Genome Size and Ploidy Level

The genome sizes of collected accessions (Table 1) were estimated by flow cytometry using the F. ornus (2C-value = 1.98 pg) as reference standard. Nuclei isolated from a single mature leaf were analyzed in three technical replicates for each accession of set #1. The analysis was carried out with a Partec PAS flow cytometer (Partec, http://www.partec.de/), equipped with a mercury lamp. Fully expanded leaves (1 cm2) were chopped in a glass Petri dish with 1 mL nuclei extraction buffer OTTO1 [45] and 3 drops of Tween 20. After 3 min, 1 mL of OTTO2 [45] supplemented with DAPI (4 µg/mL) was added. The solution was filtered through a 30 μm Cell-Trics disposable filter (Partec). The relative fluorescence intensity of stained nuclei was measured on a linear scale, and 4000–5000 nuclei for each sample were analyzed. DNA content histograms were generated using the Partec software package (Partec-FlowMax®, Münster, Germany).

2.4. DNA Extraction and Genotyping

Genomic DNA was extracted from 100 mg of powdered, frozen, young leaf tissue of each individual from sample set #1 using the QiagenDNeasy Plant Mini Kit (Qiagen, Hilden, Germany). The purity and quantity of the DNA extracts were assessed with a NanoDrop 1000 spectrophotometer (Thermo Scientific, Waltham, MA, USA). Molecular investigations were carried out by amplifying 6 plastid (chloroplast) microsatellite (SSR, simple sequence repeat) markers (cpSSR) (ccmp2, ccmp3, ccpm4, ccmp6, ccmp7, and ccmp10 [46]), 3 plastid DNA regions (atpB-rbcL, CPFRAX6 and matK [33]) and 11 nuclear microsatellite nSSR (FEMSATL4, FEMSATL11, FEMSATL12, FEMSATL16, FEMSATL19 [47], M230 [48], EST-SSR326, EST-SSR427, EST-SSR431, EST-SSR520, EST-SSR528 [49]) markers, respectively. PCR reactions were performed following the procedures reported in Garfì et al. (2013) [50], using primers fluorescently labelled with FAM, VIC, NED and PET. The fragments were separated by capillary electrophoresis using an ABI PRISM 3130 Genetic Analyzer (Applied Biosystems) to detect length polymorphism only. Fragments were sized and binned into alleles using Gene Mapper v. 4.1 software (Thermo Fisher Scientific, Waltham, MA, USA), (Applied Biosystems) (Table S2).

2.5. Data Analysis

Plastid DNA haplotypes were defined based on the concatenation of fragment length polymorphism at cpSSRs and amplified plastid DNA regions. To assign the species of origin of the sampled materials, the obtained haplotypes were compared visually with previously published cpSSR profiles from the three European ash species reported in Heuertz et al. (2006) [4].
Genetic relationships between nSSR profiles of both sample sets (set #1; set #2) were estimated using Bruvo’s distance [51] in the poppr package [52] in R Core Team (2020; http://www.R-project.org). A dendrogram was computed from each distance matrix using the UPGMA (Unweighted Pair Group Method with Arithmetic Mean) implemented in the adegenet package [53] in R. Bootstrap analysis was performed based on 1000 replicate samples to assess the robustness of the inferred evolutionary relationships in the dendrogram.
After establishing that Sicilian manna ash is F. angustifolia based on the listed analysis, we assessed the genetic differentiation between Sicilian manna ash and the collection of European F. angustifolia, F. excelsior and their hybrids using Wright’s fixation index (Fst) [54] and Nei’s (1973) distance [55] computed through hierfstat [56] in R. The genetic variability across F. angustifolia (FAN accessions belonging to set #2 was estimated using the observed (Ho) and expected (He) heterozygosities [55], Shannon’s index (I) and the inbreeding coefficient (Fis) for sampling locations in GenAlEx 6.5 [57]. Each locus and population was tested for Hardy-Weinberg equilibrium deviation with the exact test through Genepop v. 3.4 [58], with the default parameters (dememorization = 10,000, number of batches = 100, and number of iterations/batch = 5000). To compare the genetic diversity of population studied with different sample sizes the allelic richness (AR) within sampling locations was also evaluated though SPAGeDi software [59]. Population pairwise fixation index (Fst) values were then computed for only F. angustifolia accessions, grouped based on their sampling location or country and a neighbor-joining (NJ) tree using was developed using the adegenet package [53].
Finally, to evaluate the genetic structure of F. angustifolia distributed across Europe (belonging to set #2 a discriminant analysis of principal components (DAPCs) was employed. Samples belonging to F. angustifolia were grouped based on their geographic area of origin (in five main groups: Balkans, Eastern Europe, France, Italy and Portugal) and DAPC analysis, implemented in the adegenet package [53], was carried out to infer population subdivision of the germplasm studied. The number of principal components (PCs) retained was evaluated using the cross-validation procedure. The K-means algorithm “find.clusters” was used to independently verify the assignment of individuals to clusters.

3. Results

Ploidy level, DNA content and morphological trait variation of the manna ash collection DNA content of the 34 accessions belonging to the manna ash collection and of four F. ornus individual trees (set #1) was estimated based on the relative intensity of fluorescence using the known F. ornus genome size (1.98) as reference [60]. DNA content estimates were congruent with all individuals of set #1 being diploids (2n = 2 × = 46) [61]. Flow cytometry-derived genome sizes (pg/2C) for manna ash varieties ranged from 1.539 to 1.544 (Table 1).
Broad variability in several phenotypic traits related to leaf morphology, inflorescence and infructescence features were observed among the different local varieties belonging to the Sicilian manna ash germplasm collection (Table S1). Leaf shape, number of leaflets, leaflet margin, petiole length and rachis wings were highly variable (Table S1). Also the inflorescences showed a great range of variation. Differences between varieties were mainly observed in the structure of reproductive organs, including the terminal clustering of multiple carpels, the partial basal fusion of individual carpels and the attachment and orientation of the seeds (Table S1). The mean values of some morphological traits showed most high variability between the manna ash collection and the F. ornus reference trees (Table 1). Specifically, the largest phenotypic variability was found in the number of samaras/raceme (5.8 vs. 46.0), followed by samara stalk length (1.1 vs. 0.4) and apical leaf length/width ratio (0.28 vs. 0.52) (Table 1). Moreover, flowering time (November–January for manna ash vs. May–June for F. ornus) and the colour of apical buds (red in manna ash vs. white in F. ornus) were clearly distinct for manna ash and F. ornus (Table 1).

3.1. Genetic Variation of Plastid DNA Microsatellites (cpSSRs) and Amplified Regions in the Manna Ash Collection

Five (ccmp3, ccmp4, ccmp7, atpB/rbcL and matK) out of nine plastid DNA markers were monomorphic in set #1, displaying fragment lengths of 97, 140, 117, 157 and 253 bp, respectively. The other loci showed low but significant levels of polymorphism (Table 2): Three size variants, with amplification fragment sizes of 364, 365 and 366 bp, were observed at CPFRAX6, whereas two distinct size variants separated by one and four nucleotides were showed at ccmp6 and ccmp2, respectively. Finally, ccmp10 displayed three specific size variants, with amplicons of 103, 104 and 106 bp (Table 2), respectively. The size variants combined into a total of 4 haplotypes (Table 2). Except for “Verdello”, the samples belonging to each local variety showed one specific haplotype. The four haplotypes detected in set #1 represented three of the twenty-two previously characterized cpSSR-based haplotypes [4]: Manna ash accessions carried either a sub-variant of H5 (92% of accessions) or haplotype H10 (8% of accessions), these haplotypes having previously been observed in F. angustifolia and in F. excelsior; the F. ornus reference trees carried H19, a haplotype private to F. ornus (Table 2).

3.2. Genetic Diversity of Manna Ash Germplasm

The genetic diversity of the manna ash germplasm and F. ornus genotypes, the so called set #1, was investigated using 11 nSSR (Table S2). Phylogenetic analysis based on Bruvo’s distance and the UPGMA algorithm generated a dendrogram that comprised four main clusters across set #1 (Figure 1). A total of 20 unique SSR profiles were detected (16 from manna ash collection and 4 for F. ornus accessions, respectively), with “Frassino monumentale” as the most distant sample among the manna ash genotypes. Except for varieties “Baciciu”, “Macigna” and “Nsiriddu”, all accessions were assigned to their expected local variety (Figure 1), showing “Verdello” as the local variety with the highest genetic variability. In addition, the accessions analyzed belonging to “Sarvaggio”, “Nivuru”, “Russo” and “Abbassa cappeddu” can be considered clones, respectively, showing the same genetic profile within the same variety. The four reference trees of F. ornus grouped together in a cluster that behaved like an outgroup.

3.3. Genetic Diversity of Fraxinus spp. in Europe

In order to compare the genetic relationships and diversity between the manna ash collection (sample set #1) and the germplasm of F. angustifolia and F. excelsior throughout the partially overlapping natural distribution ranges of both species across Europe, we combined our SSR profiles of manna ash with the genotypic profiles described in Gérard et al. (2013) [14] into a second dataset called sample set #2, which included 495 unique profiles at 11 SSRs. UPGMA analysis based on Bruvo’s distance [51] identified groups based on species (Figure 2; Table S2). Indeed, three main clusters were highlighted, with two branches represented almost exclusively by F. angustifolia and F. excelsior samples, respectively. As expected, samples belonging to F. ornus clustered as the most distant genotypes, behaving as outgroup, while the individuals morphologically classified as hybrids were distributed across the two main groups. Interestingly, F. angustifolia samples coming from Southern Italian regions from Gérard et al. (2013) [14] data clustered together with genotypes of our manna ash collection (Figure 2), highlighting a distinctive, basal position of Southern Italian F. angustifolia germplasm in comparison with the range-wide collection of the species.
Interestingly, within FAN, samples collected in Southern Italy (Sicily and Calabria) showed lower genetic distance (Nei, 1973 [55]) and lower Fst values with respect to the other FAN populations collected in Europe, whereas comparison to FEX populations resulted in higher values (Table 3). Hybrids of both ash species were closer both to FAN (Fst = 0.030; Nei = 0.159) and FEX (Fst = 0.028; Nei = 0.110) than to FAN (Italy) (Fst = 0.107; Nei = 0.536) (Table 3).
Different genetic parameters (I, He, Ho, Fis, AR and Fst) were also estimated for F. angustifolia sampling locations belonging to set #2 (Table 4). Hungary and France2 locations had, respectively, the lowest (0.504) and highest (0.680) values for genetic diversity (He). Overall, genetic diversity parameters (I, He, Ho) displayed similar values across the locations studied (Table 4). Sixteen out of twenty-one locations showed an excess of heterozygotes, showing a negative inbreeding coefficient (Fis). However, except Hungary population (−0.607), Fis was close to zero therefore all groups could be considered in equilibrium (Table 4).
Overall allelic richness (AR) ranged from 1.173 (SSR431) to 3.746 (Fem12) for SSR431 and Fem12 markers, respectively (Table S3). AR was higher in trees collected in Turkey (3.55) than the other populations. Macedonia, Montenegro, Portugal1, five out of seven French groups and the two population collected in Serbia showed similar AR values (ranging from 3.05 to 3.42), while population belonging to Hungary had the lowest value (2.28; Table 4).
The Fst values were also used to assess the genetic relationships across the population belonging to the F. angustifolia collection here studied (Figure 3; Table S4). Three main clusters were observed in the NJ-tree: six out of seven populations collected in France were gathered together with the two Italian groups and Portugal2 population; except the samples collected in Croatia, the other Balkan populations clustered with samples belonging to Turkey and Hungary; and, finally, the remaining populations of France (France7), Balkans (Croatia1 and 2) and Portugal (Portugal1) were linked to Bulgaria and Ukraine populations (Figure 3). On the other hand, comparing the Fst recorded on samples grouped by country, the greatest distance was observed between the pair Hungary–Bulgaria; except Croatia, the populations belonging to Balkan clustered close in the NJ-tree. Portugal and France were genetically separated, with the last population near the branch that gathered Turkey and Italy (Figure S1).
DAPC identified five clusters corresponding to the five groups selected (Figure 4). Clusters including the samples belonging to France and Portugal were overlapping, as well as clusters containing Balkans and Eastern European genotypes. On the contrary all samples collected in Italy (from Calabria and Sicily) were separated from the other groups. Except for some samples, the plot of the first two principal components distinguished clearly three groups represented by genotypes from Eastern, Western and Mediterranean Europe, respectively (Figure 4).

4. Discussion

The genetics of endangered Fraxinus spp. populations is of great interest for both conservation and evolutionary aspects. Using a multidisciplinary approach, including molecular analysis, we demonstrated in this study that an important and residual manna ash germplasm collection located in the Madonie Mountains (Sicily, Italy), belongs to F. angustifolia, the narrow-leaved ash. We also showed that this population contained high genetic diversity and, together with a population from Calabria, was strongly differentiated from F. angustifolia populations from other locations in Europe (Balkans, Eastern Europe, France, and Portugal). The assessment of the genetic diversity is crucial to plan activities aimed to conservation of this important and endangered forest tree genetic resource.
Notwithstanding the limited number of individuals studied, plants belonging to the manna ash collection analyzed showed a wide variation in several phenotypic traits, such as leaf characteristics, inflorescence and infructescence features, plant vigor and morphology, showing a continuous and narrow range of values for individual traits. Leaf morphology is the strongest differentiating character within the local collection, although this trait is not successfully used to characterize the varieties, being strongly influenced by environmental factors. Indeed, it is well known that plants react to water stress, which is particularly strong in the Mediterranean area, by modifying their leaf traits. Considering that the trees collected come from a heterogeneous mountain environment in which neighboring individuals compete for the same ground and light resources, the observed phenotypic variations might be attributed to the impact of environmental factors on growth habit. Regarding fruit morphology, the shape and the length of the fruits of “manna” varieties were quite heterogeneous, as well as the colour or samaras changing from light green of most cultivars to veined brown of “Nsiriddu”. These traits; thus, showed a weak distinguishing power [62]. Nevertheless distinctive morphological traits separated all manna ash varieties from F. ornus. Specifically, in the local varieties the samara stalk length was greater (nearly three times) than in F. ornus, while the apical leaf length/width ratio and the number of samaras/raceme of manna ash samples were approximately two and a half and eight times lower, respectively, separating the two groups compared. Variety identification based on morphological data can be verified using molecular analysis, because the environmental effects, epistatic interactions and pleiotropic effects can interfere with morphological traits evaluation, as in many forest trees [63].
The genome size showed a small change in the 2C nuclear DNA content within the samples belonging to the manna ash collection (from 1.539 to 1.544 pg). The existence of intraspecific variation in genome size has been reported in several plant species [64,65,66]. However, due to the little shift here reported, the genome size, as well as the ploidy level, can be considered stable in our collection, as commonly observed within the species [67]. The variations recorded can be explained by technical issues, as reported for some angiosperms [68,69]. The 2C DNA values observed in the manna ash collection unambiguously assign the manna germplasm to F. angustifolia (1.540 pg [60]) and are different from both F. excelsior (1.68 pg; [60]), and F. ornus (1.98 pg; [60]), showing a larger genome size due to probably a high number of repetitive elements and/or several ribosomal gene repetitions [60].
Molecular analyses confirmed the differences highlighted through morphological and cytological approaches. In agreement with the low chloroplast DNA mutation rate detected in the Oleaceae [70], cpSSRs and plastid DNA regions identified a low genetic diversity in the manna ash collection, identifying three haplotypes, two sub-variants of H5 (covering 92% of samples) and H10 (the remaining 8%), respectively. The haplotype detected in the reference trees (H19) was previously found only in F. ornus, specifically in trees from Italy and Corsica. In agreement with the increased botanical similarity of F. angustifolia and F. excelsior and a partially overlapping phenology [6,71,72], an extensive sharing of cpDNA haplotypes between F. angustifolia and F. excelsior has been found previously but without common profiles between them and F. ornus [4]. Indeed, both H5 and H10 variants have been shown to be shared haplotypes between F. angustifolia and F. excelsior although in different geographic regions [4,73]. The majority of manna ash accessions carried haplotype H05, a haplotype observed in F. angustifolia throughout central and southern Italy and in F. excelsior in a restricted area of the Eastern Alps; this particular distribution could be related to two possible different and independent glacial refuges of ash species [73]. The other haplotype (H10) observed in “Abbassa cappeddu” variety and in some trees belonging to “Verdello” was detected in F. angustifolia trees collected in Portugal and Corsica [4] and only in the Czech Republic for F. excelsior.
Microsatellites are reported as very effective marker in terms of high information content and discrimination power owing to high allelic variation and allowing clear identification of populations or varieties in several plant species [74,75,76,77]. Nuclear SSR (nSSR) profiles showed a noteworthy rate of polymorphism and, except for “Baciciu” and “Cavolo”, were able to group each accession with its own variety. The most represented local variety named “Verdello” was grouped in a main cluster, together with tree belonging to “Nsiriddu”, showing a high variability, in agreement to the profiles obtained in natural populations of F. angustifolia in Greece [78]. Among studied varieties, “Verdello” and “Nsiriddu” showed an upright growth habit and are considered the most productive ones [18], yielding high quality manna with very similar chemical and organoleptic characteristics.
Although only a slight genetic differentiation between F. angustifolia and F. excelsior was reported [79,80], our findings highlighted a clear separation between trees belonging to two species collected throughout their natural distribution across Europe. Significant patterns of distance were found among species, with F. ornus clearly behaving like outgroup. Interestingly, a private branch grouping only F. angustifolia trees collected in the South of Italy, including the profiles recorded for manna ash collection, was highlighted. In agreement to cluster analysis, the pairwise fixation index (Fst) highlighted a clear distinctness for the populations from Southern Italy, close to Turkish and French populations. In addition both cluster and Fst analysis allowed to separate the two Italian populations highlight the feature belonging to manna ash collection. Our results are consistent with Fraxinus spp. distribution, indeed common ash (F. excelsior) is found mainly in the north regions throughout Europe [4,81] and has expanded its range in the south probably during cooler climate episodes, maintaining the current relic populations in temperate locations such as the Elburz Mountains (Turkey), Calabria (Italy), and in Sicily, more specifically in the Nebrodi Mountains, where a small population (200 plants) of F. excelsior spp. siciliensis [82,83] is located in three different sites (Caronia, Longi and Alcara Li Fusi), showing specific features (e.g., reduced size and blooming at the same time of leaf emission; [84] due to the high isolation. On the contrary, F. angustifolia is mostly restricted to the Mediterranean region [81] and the favorable environmental conditions allowed this species to spread in the Sicilian Nebrodi Mountains, giving rise at the end of 19th century more than 16 varieties distinguished for both morphological traits and manna production [21,85]. The remarkable diversity and strong genetic structure in the Sicilian collection of F. angustifolia highlighted by both cp and nSSRs probably is related to the geographic isolation in which they have been found for about 10,000 years starting from the end of the last glaciation. This trend of speciation in Fraxinus, related to specific geographic zones, is in agreement to previous work [71], and would be driven by geological and climatic modifications [86] as reported for other species [87]. Phylogenetic analysis showed also a distribution of hybrids (HYB) within both F. excelsior and F. angustifolia groups, reflecting the sharing of haplotypes between the two species [4]. More interestingly, in the last group the hybrids and trees belonging to common ash were linked to F. angustifolia trees collected in Balkan and Eastern Europe, in agreement to the species distribution [4], whereas the samples from Southern Italy were the most genetically distant plants. Our finding can be explained by the marked different flowering time that characterizes the two species in Sicily making the interspecific cross unfavorable.
Finally, grouping the F. angustifolia trees studied on the grounds of their geographic area, discriminant analysis based on nuclear microsatellites underlined a gradient from west to east in Y-axis. This evidence is consistent with the classification of F. angustifolia that can be grouped into three geographic subspecies: (i) F. angustifolia Vahl ssp. angustifolia (Portugal and the Western Mediterranean), (ii) ssp. oxycarpa (M. Bieb. ex Willd.) Franco and Rocha Afonso (Northeast Spain to Turkey), and (iii) ssp. syriaca (Boiss.) Yalt (Turkey and Asia Minor) [6,7,8]. Additionally, samples belonging to Calabria and Sicily were separated from the others. The clear diversity harbored by F. angustifolia populations from South Italy, allow to hypothesize a possible glacial refuge of species in this area, according to a temperature increasing during the late glacial maximum (18,000 years bp) in the Mediterranean eastern compared to western one, as already reported for the Turkish populations [4,88].

5. Conclusions

In summary, using a multidisciplinary approach the present study was focused to characterize in depth a historical manna ash collection represented by local varieties collected in the Madonie area (Sicily, Italy), in order to safeguard an important cultural heritage. Our finding definitively clarifies that the local varieties actually used for manna production belong to F. angustifolia. This study provides useful information for germplasm management, finalized to improve the production and productivity of agroforestry species investigated. In addition, the evidences here reported suggest the presence of an additional glacial refuge for F. angustifolia in Italy, confirming the importance of Sicily as source of biodiversity. Furthermore, our study could represent an invitation for botanists to expand the historical knowledge of the collection. Due to the importance of ash germplasm studied, all local varieties were propagated in two repository fields, at the Professional Institute for Agriculture and the Environment (I.P.A.A.) “Luigi Failla Tedaldi” (Castelbuono, Italy) and at the private Schicchi’s repository located in the Croce-Foresta district (Castelbuono, Italy) (info at [email protected]) making available this genetic resources for future breeding programs and to develop future national/international collaborations.

Supplementary Materials

The following are available online at https://www.mdpi.com/2223-7747/9/8/1035/s1, Table S1: Morphological traits of studied samples, belonging to manna ash collection and samples belonging to F. ornus, used as reference. In brackets the number of samples analyzed belonging to each local variety/species. Three replicates for each trait were analyzed. Table S2: Nuclear SSR profiles of samples belonging to (A) set #1 and (B) set #2. Table S3: Allelic richness (AR) evaluated for FAN accessions grouped based on sampling location. In the table geographic coordinates (Long and Lat) and AR values for each nSSR were indicated. Table S4: Pairwise population Fst values. Figure S1: Neighbor-joining (NJ) tree based on population pairwise fixation index. Genetic distances were computed among populations grouped based on country of origin.

Author Contributions

Conceptualization, L.A., F.M., S.F.d.B. and R.S.; Data curation, L.A., F.M. and M.H.; Formal analysis, L.A. and F.M.; Funding acquisition, R.S.; Investigation, L.A. and F.M.; Resources, G.D.N. and R.S.; Supervision, F.M.; Writing-original draft, L.A., F.M., M.H. and S.F.d.B.; Writing-review & editing, L.A., F.M., G.D.N., M.H., F.C., S.F.d.B. and R.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The authors are grateful to Maria Luisa Virga (Assessorato dell’Agricoltura, dello Sviluppo Rurale e della Pesca Mediterranea-Dipartimento Regionale dell’Agricoltura-Regione Sicilia) for encouraging the meeting between the research groups.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wallander, E.; Albert, V.A. Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data. Am. J. Bot. 2000, 87, 1827–1841. [Google Scholar] [CrossRef] [PubMed]
  2. Hinsinger, D.D.; Gaudeul, M.; Couloux, A.; Bousquet, J.; Frascaria-Lacoste, N. The phylogeography of Eurasian Fraxinus species reveals ancient transcontinental reticulation. Mol. Phylogenet. Evol. 2014, 77, 223–237. [Google Scholar] [CrossRef] [PubMed]
  3. Wallander, E. Systematics of Fraxinus (Oleaceae) and evolution of dioecy. Plant Syst. Evol. 2008, 273, 25–49. [Google Scholar] [CrossRef]
  4. Heuertz, M.; Carnevale, S.; Fineschi, S.; Sebastiani, F.; Hausman, J.F.; Paule, L.; Vendramin, G.G. Chloroplast DNA phylogeography of European ashes, Fraxinus sp. (Oleaceae): Roles of hybridization and life history traits. Mol. Ecol. 2006, 15, 2131–2140. [Google Scholar] [CrossRef] [PubMed]
  5. Picard, J.-F. Contribution à l’étude de la biologie florale et de la fructification du Frêne commun (Fraxinus excelsior L.). Rev. For. Fr. 1982, 97. [Google Scholar] [CrossRef] [Green Version]
  6. Wallander, E. Evolution of Wind-Pollination in Fraxinus (Oleaceae): An Ecophylogenetic Approach. Ph.D. Thesis, Göteborg University, Göteborg, Sweden, 2001. [Google Scholar]
  7. Tutin, T.G.; Heywood, V.H.; Burges, N.A.; Moore, D.M.; Valentine, D.H.; Walters, S.M.; Webb, D.E.; Chater, A.O.; Defilipps, R.A.; Richardson, I.B.K.; et al. Flora Europaea: Plantaginaceae to Compositae (and Rubiaceae); Cambridge University Press: Cambridge, UK, 1972. [Google Scholar]
  8. Huntley, B.; Birks, H.J.B.; Harry, J.B. Atlas of Past and Present Pollen Maps for Europe, 0–13,000 Years Ago; Cambridge University Press: Cambridge, UK, 1983; ISBN 978-0-521-23735-2. [Google Scholar]
  9. Temunović, M.; Franjić, J.; Satovic, Z.; Grgurev, M.; Frascaria-Lacoste, N.; Fernández-Manjarrés, J.F. Environmental Heterogeneity Explains the Genetic Structure of Continental and Mediterranean Populations of Fraxinus angustifolia Vahl. PLoS ONE 2012, 7, e42764. [Google Scholar] [CrossRef] [Green Version]
  10. FRAXIGEN, 2005 Ash Species in Europe: Biological Characteristics and Practical Guidelines for Sustainable Use—ProQuest. Available online: https://search.proquest.com/openview/e333985a9ac22793988179029545b7da/1?pq-origsite=gscholarandcbl=29663 (accessed on 17 June 2020).
  11. Thomas, P.A. Biological Flora of the British Isles: Fraxinus excelsior. J. Ecol. 2016, 104, 1158–1209. [Google Scholar] [CrossRef]
  12. Caudullo, G.; Houston Durrant, T. Fraxinus angustifolia in Europe: Distribution, habitat, usage and threats. In European Atlas of Forest Tree Species 2016; San-Miguel-Ayanz, J., de Rigo, D., Caudullo, G., Houston Durrant, T., Mauri, A., Eds.; Publications Office of the European Union: Luxembourg, 2016; p. 97. [Google Scholar]
  13. Bogdan, S.; Kajba, D.; Franjic, J.; Idzojtic, M.; Skvorc, Z.; Trupčević, I.K. Genetic variation in quantitative traits within and among Croatian narrow-leaved ash (Fraxinus angustifolia Vahl) populations assessed in an open-pollinated progeny test. Period. Boil. 2007, 109, 1–11. [Google Scholar]
  14. Gérard, P.R.; Temunović, M.; Sannier, J.; Bertolino, P.; Dufour, J.; Frascaria-Lacoste, N.; Fernández-Manjarrés, J.F. Chilled but not frosty: Understanding the role of climate in the hybridization between the Mediterranean Fraxinus angustifolia Vahl and the temperate Fraxinus excelsior L. (Oleaceae) ash trees. J. Biogeogr. 2013, 40, 835–846. [Google Scholar] [CrossRef]
  15. Noti, R.; van Leeuwen, J.F.N.; Colombaroli, D.; Vescovi, E.; Pasta, S.; La Mantia, T.; Tinner, W. Mid- and late-Holocene vegetation and fire history at Biviere di Gela, a coastal lake in southern Sicily, Italy. Veg. Hist. Archaeobot. 2009, 18, 371–387. [Google Scholar] [CrossRef] [Green Version]
  16. Médail, F.; Diadema, K. Glacial refugia influence plant diversity patterns in the Mediterranean Basin. J. Biogeogr. 2009, 36, 1333–1345. [Google Scholar] [CrossRef]
  17. Mazzola, P.; Schicchi, R.; Spadaro, V. Ricerche finalizzate al recupero e conservazione del germoplasma dei frassini da manna sulle Madonie (Sicilia settentrionale). In Proceedings of the 101 Congresso Società Botanica Italiana, Caserta, Italy, 27–29 September 2006; p. 137. [Google Scholar]
  18. Schicchi, R.; Camarda, L.; Spadaro, V.; Pitonzo, R. Caratterizzazione chimica della manna estratta nelle Madonie (Sicilia) da cultivar di Fraxinus angustifolia e di Fraxinus ornus (Oleaceae). Quad. Bot. Amb. Appl. 2006, 17, 151–174. [Google Scholar]
  19. Giardinieri, A.; Schicchi, R.; Geraci, A.; Rosselli, S.; Maggi, F.; Fiorini, D.; Ricciutelli, M.; Loizzo, M.R.; Bruno, M.; Pacetti, D. Fixed oil from seeds of narrow-leaved ash (F. angustifolia subsp. angustifolia): Chemical profile, antioxidant and antiproliferative activities. Food Res. Int. 2019, 119, 369–377. [Google Scholar] [CrossRef]
  20. Guarcello, R.; Gaglio, R.; Todaro, A.; Alfonzo, A.; Schicchi, R.; Cirlincione, F.; Moschetti, G.; Francesca, N. Insights Into the Cultivable Microbial Ecology of “Manna” Ash Products Extracted From Fraxinus angustifolia (Oleaceae) Trees in Sicily, Italy. Front. Microbiol. 2019, 10, 984. [Google Scholar] [CrossRef]
  21. Minà Palumbo, F. Monografia sulla coltivazione del frassino. Agric. Lal. 1876, 1875, 19–25. [Google Scholar]
  22. Falci, R. Il frassino da manna in Sicilia. Boll. R. Orto Bot. Giard. Col. Palermo 1910, 9, 145–168. [Google Scholar]
  23. Weber, J.L. Informativeness of human (dC-dA) n (dG-dT) n polymorphisms. Genomics 1990, 7, 524–530. [Google Scholar] [CrossRef]
  24. Morgante, M.; Olivieri, A.M. PCR-amplified microsatellites as markers in plant genetics. Plant J. 1993, 3, 175–182. [Google Scholar] [CrossRef]
  25. Bacchi, M.; Leone, M.; Mercati, F.; Preiti, G.; Sunseri, F.; Monti, M. Agronomic Evaluation and Genetic Characterization of Different Accessions in Lentil (Lens culinaris Medik.). Ital. J. Agron. 2010, 5, 303. [Google Scholar] [CrossRef]
  26. Jiao, Y.; Jia, H.; Li, X.; Chai, M.; Jia, H.; Chen, Z.; Wang, G.; Chai, C.; van de Weg, E.; Gao, Z. Development of simple sequence repeat (SSR) markers from a genome survey of Chinese bayberry (Myrica rubra). BMC Genom. 2012, 13, 201. [Google Scholar] [CrossRef] [Green Version]
  27. Mercati, F.; Longo, C.; Poma, D.; Araniti, F.; Lupini, A.; Mammano, M.M.; Fiore, M.C.; Abenavoli, M.R.; Sunseri, F. Genetic variation of an Italian long shelf-life tomato (Solanum lycopersicon L.) collection by using SSR and morphological fruit traits. Genet. Resour. Crop Evol. 2015, 62, 721–732. [Google Scholar] [CrossRef]
  28. Mercati, F.; Catarcione, G.; Paolacci, A.R.; Abenavoli, M.R.; Sunseri, F.; Ciaffi, M. Genetic diversity and population structure of an Italian landrace of runner bean (Phaseolus coccineus L.): Inferences for its safeguard and on-farm conservation. Genetica 2015, 143, 473–485. [Google Scholar] [CrossRef] [PubMed]
  29. King, R.A.; Ferris, C. Chloroplast DNA phylogeography of Alnus glutinosa (L.) Gaertn. Mol. Ecol. 1998, 7, 1151–1161. [Google Scholar] [CrossRef]
  30. Palmé, A.E. Chloroplast DNA variation, postglacial recolonization and hybridization in hazel, Corylus avellana. Mol. Ecol. 2002, 11, 1769–1779. [Google Scholar] [CrossRef] [PubMed]
  31. Rajora, O.P.; Dancik, B.P. Chloroplast DNA inheritance in Populus. Theor. Appl. Genet. 1992, 84, 280–285. [Google Scholar] [CrossRef] [PubMed]
  32. Dumolin, S.; Demesure, B.; Petit, R.J. Inheritance of chloroplast and mitochondrial genomes in pedunculate oak investigated with an efficient PCR method. Theor. Appl. Genet. 1995, 91, 1253–1256. [Google Scholar] [CrossRef]
  33. Harbourne, M.E.; Douglas, G.C.; Waldren, S.; Hodkinson, T.R. Characterization and primer development for amplification of chloroplast microsatellite regions of Fraxinus excelsior. J. Plant Res. 2005, 118, 339–341. [Google Scholar] [CrossRef]
  34. Erichsen, E.O.; Budde, K.B.; Sagheb-Talebi, K.; Bagnoli, F.; Vendramin, G.G.; Hansen, O.K. Hyrcanian forests—Stable rear-edge populations harbouring high genetic diversity of Fraxinus excelsior, a common European tree species. Divers. Distrib. 2018, 24, 1521–1533. [Google Scholar] [CrossRef] [Green Version]
  35. Kellogg, E.A. Relationships of cereal crops and other grasses. PNAS 1998, 95, 2005–2010. [Google Scholar] [CrossRef] [Green Version]
  36. Leitch, I.J.; Chase, M.W.; Bennett, M.D. Phylogenetic Analysis of DNA C-values Provides Evidence for a Small Ancestral Genome Size in Flowering Plants. Ann. Bot. 1998, 82, 85–94. [Google Scholar] [CrossRef]
  37. Doležel, J.; Bartoš, J. Plant DNA Flow Cytometry and Estimation of Nuclear Genome Size. Ann. Bot. 2005, 95, 99–110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Doležel, J.; Greilhuber, J.; Suda, J. Estimation of nuclear DNA content in plants using flow cytometry. Nat. Protoc. 2007, 2, 2233–2244. [Google Scholar] [CrossRef] [PubMed]
  39. Petrov, D.A.; Sangster, T.A.; Johnston, J.S.; Hartl, D.L.; Shaw, K.L. Evidence for DNA Loss as a Determinant of Genome Size. Science 2000, 287, 1060–1062. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Bennetzen, J.L.; Ma, J.; Devos, K.M. Mechanisms of Recent Genome Size Variation in Flowering Plants. Ann. Bot. 2005, 95, 127–132. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Harkess, A.; Mercati, F.; Abbate, L.; McKain, M.; Pires, J.C.; Sala, T.; Sunseri, F.; Falavigna, A.; Leebens-Mack, J. Retrotransposon Proliferation Coincident with the Evolution of Dioecy in Asparagus. G3 Genes Genomes Genet. 2016, 6, 2679–2685. [Google Scholar] [CrossRef]
  42. Murray, B.G. When does Intraspecific C-value Variation become Taxonomically Significant? Ann. Bot. 2005, 95, 119–125. [Google Scholar] [CrossRef] [Green Version]
  43. Garnatje, T.; Garcia, S.; Vilatersana, R.; Vallès, J. Genome Size Variation in the Genus Carthamus (Asteraceae, Cardueae): Systematic Implications and Additive Changes During Allopolyploidization. Ann. Bot. 2006, 97, 461–467. [Google Scholar] [CrossRef] [Green Version]
  44. Raimondo, F.M.; Bonomo, R.; Lentini, F. Il frassino da manna in Sicilia, pianta officinale da rivalutare. Giorn. Bot. Ital. 1980, 114, 141–142. [Google Scholar]
  45. Otto, F.J. Preparation and Staining of Cells for High-Resolution DNA Analysis. In Flow Cytometry and Cell Sorting; Radbruch, A., Ed.; Springer: Berlin/Heidelberg, Germany, 1992; pp. 65–68. ISBN 978-3-662-02785-1. [Google Scholar]
  46. Weising, K.; Gardner, R.C. A set of conserved PCR primers for the analysis of simple sequence repeat polymorphisms in chloroplast genomes of dicotyledonous angiosperms. Genome 1999, 42, 9–19. [Google Scholar] [CrossRef]
  47. Lefort, F.; Brachet, S.; Frascaria-Lacoste, N.; Edwards, K.J.; Douglas, G.C. Identification and characterization of microsatellite loci in ash (Fraxinus excelsior L.) and their conservation in the olive family (Oleaceae). Mol. Ecol. 1999, 8, 1088–1089. [Google Scholar] [CrossRef]
  48. Brachet, S.; Jubier, M.F.; Richard, M.; Jung-Muller, B.; Frascaria-Lacoste, N. Rapid identification of microsatellite loci using 5′ anchored PRC in the common ash Fraxinus excelsior. Mol. Ecol. 1999, 8, 160–163. [Google Scholar]
  49. Aggarwal, R.K.; Allainguillaume, J.; Bajay, M.M.; Barthwal, S.; Bertolino, P.; Chauhan, P.; Consuegra, S.; Croxford, A.; Dalton, D.L.; Belder, E.D.; et al. Permanent Genetic Resources added to Molecular Ecology Resources Database 1 August 2010–30 September 2010. Mol. Ecol. Resour. 2011, 11, 219–222. [Google Scholar] [CrossRef] [PubMed]
  50. Garfì, G.; Mercati, F.; Fontana, I.; Collesano, G.; Pasta, S.; Vendramin, G.G.; De Michele, R.; Carimi, F. Habitat features and genetic integrity of wild grapevine Vitis vinifera L. subsp. sylvestris (C.C. Gmel.) Hegi populations: A case study from Sicily. Flora Morphol. Distrib. Funct. Ecol. Plants 2013, 208, 538–548. [Google Scholar] [CrossRef]
  51. Bruvo, R.; Michiels, N.K.; D’souza, T.G.; Schulenburg, H. A simple method for the calculation of microsatellite genotype distances irrespective of ploidy level. Mol. Ecol. 2004, 13, 2101–2106. [Google Scholar] [CrossRef] [PubMed]
  52. Kamvar, Z.N.; Tabima, J.F.; Grünwald, N.J. Poppr: An R package for genetic analysis of populations with clonal, partially clonal, and/or sexual reproduction. PeerJ 2014, 2, e281. [Google Scholar] [CrossRef] [Green Version]
  53. Jombart, T.; Ahmed, I. Adegenet 1.3-1: New tools for the analysis of genome-wide SNP data. Bioinformatics 2011, 27, 3070–3071. [Google Scholar] [CrossRef] [Green Version]
  54. Wright, S. The Interpretation of Population Structure by F-Statistics with Special Regard to Systems of Mating. Evolution 1965, 19, 395–420. [Google Scholar] [CrossRef]
  55. Nei, M. Analysis of Gene Diversity in Subdivided Populations. PNAS 1973, 70, 3321–3323. [Google Scholar] [CrossRef] [Green Version]
  56. Goudet, J. Hierfstat, a package for r to compute and test hierarchical F-statistics. Mol. Ecol. Notes 2005, 5, 184–186. [Google Scholar] [CrossRef] [Green Version]
  57. Peakall, R.; Smouse, P.E. genalex 6: Genetic analysis in Excel. Population genetic software for teaching and research—An update. Bioinformatics 2012, 28, 2537–2539. [Google Scholar] [CrossRef] [Green Version]
  58. Raymond, M.; Rousset, F. An Exact Test for Population Differentiation. Evolution 1995, 49, 1280–1283. [Google Scholar] [CrossRef] [PubMed]
  59. Hardy, O.J.; Vekemans, X. Spagedi: A versatile computer program to analyse spatial genetic structure at the individual or population levels. Mol. Ecol. Notes 2002, 2, 618–620. [Google Scholar] [CrossRef] [Green Version]
  60. Siljak-Yakovlev, S.; Temunović, M.; Robin, O.; Raquin, C.; Frascaria-Lacoste, N. Molecular–cytogenetic studies of ribosomal RNA genes and heterochromatin in three European Fraxinus species. Tree Genet. Genomes 2014, 10, 231–239. [Google Scholar] [CrossRef]
  61. Ivanova, D.; Dimitrova, D.; Vladimirov, V. Chromosome numbers of selected woody species from the Bulgarian. Phytol. Balc. 2006, 12, 79–84. [Google Scholar]
  62. Jarni, K.; Westergren, M.; Kraigher, H.; Brus, R. Morphological variability of Fraxinus angustifolia Vahl in the north-western Balkans. Acta Soc. Bot. Pol. 2011, 80, 245–252. [Google Scholar] [CrossRef] [Green Version]
  63. Ziegenhagen, B.; Fladung, M. DNA Markers for Identification and Evaluation of Genetic Resources in Forest Trees: Case Studies in Abies, Picea and Populus. In Molecular Marker Systems in Plant Breeding and Crop Improvement; Lörz, H., Wenzel, G., Eds.; Springer: Berlin/Heidelberg, Germany, 2005; pp. 413–429. ISBN 978-3-540-26538-2. [Google Scholar]
  64. Schmuths, H.; Meister, A.; Horres, R.; Bachmann, K. Genome Size Variation among Accessions of Arabidopsis thaliana. Ann. Bot. 2004, 93, 317–321. [Google Scholar] [CrossRef] [Green Version]
  65. Wang, Y.; Bigelow, C.A.; Jiang, Y. Ploidy Level and DNA Content of Perennial Ryegrass Germplasm as Determined by Flow Cytometry. HortScience 2009, 44, 2049–2052. [Google Scholar] [CrossRef] [Green Version]
  66. Díez, C.M.; Gaut, B.S.; Meca, E.; Scheinvar, E.; Montes-Hernandez, S.; Eguiarte, L.E.; Tenaillon, M.I. Genome size variation in wild and cultivated maize along altitudinal gradients. New Phytol. 2013, 199, 264–276. [Google Scholar] [CrossRef] [Green Version]
  67. Eilam, T.; Anikster, Y.; Millet, E.; Manisterski, J.; Sagi-Assif, O.; Feldman, M. Genome size and genome evolution in diploid Triticeae species. Genome 2007, 50, 1029–1037. [Google Scholar] [CrossRef]
  68. Greilhuber, J. Intraspecific Variation in Genome Size in Angiosperms: Identifying its Existence. Ann. Bot. 2005, 95, 91–98. [Google Scholar] [CrossRef] [Green Version]
  69. Loureiro, J.; Rodriguez, E.; Doležel, J.; Santos, C. Flow Cytometric and Microscopic Analysis of the Effect of Tannic Acid on Plant Nuclei and Estimation of DNA Content. Ann. Bot. 2006, 98, 515–527. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  70. Besnard, G.; Khadari, B.; Baradat, P.; Bervillé, A. Olea europaea (Oleaceae) phylogeography based on chloroplast DNA polymorphism. Theor. Appl. Genet. 2002, 104, 1353–1361. [Google Scholar] [CrossRef] [PubMed]
  71. Jeandroz, S.; Roy, A.; Bousquet, J. Phylogeny and Phylogeography of the Circumpolar GenusFraxinus(OLEACEAE) Based on Internal Transcribed Spacer Sequences of Nuclear Ribosomal DNA. Mol. Phylogenet. Evol. 1997, 7, 241–251. [Google Scholar] [CrossRef] [PubMed]
  72. Morand-Prieur, M.E.; Vedel, F.; Raquin, C.; Brachet, S.; Sihachakr, D.; Frascaria-Lacoste, N. Maternal inheritance of a chloroplast microsatellite marker in controlled hybrids between Fraxinus excelsior and Fraxinus angustifolia. Mol. Ecol. 2002, 11, 613–617. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  73. Brewer, S. Recolonisation Postglaciaire de Quelques Taxons Tempérés en Europe: Une Approche Spatiale et Temporelle. Ph.D. Thesis, Cornell University, Marseille, France, 2002. [Google Scholar]
  74. Thomson, M.J.; Septiningsih, E.M.; Suwardjo, F.; Santoso, T.J.; Silitonga, T.S.; McCouch, S.R. Genetic diversity analysis of traditional and improved Indonesian rice (Oryza sativa L.) germplasm using microsatellite markers. Theor. Appl. Genet. 2007, 114, 559–568. [Google Scholar] [CrossRef] [PubMed]
  75. Blair, M.W.; Díaz, L.M.; Buendía, H.F.; Duque, M.C. Genetic diversity, seed size associations and population structure of a core collection of common beans (Phaseolus vulgaris L.). Theor. Appl. Genet. 2009, 119, 955–972. [Google Scholar] [CrossRef]
  76. Carimi, F.; Mercati, F.; De Michele, R.; Fiore, M.C.; Riccardi, P.; Sunseri, F. Intra-varietal genetic diversity of the grapevine (Vitis vinifera L.) cultivar ‘Nero d’Avola’ as revealed by microsatellite markers. Genet. Resour. Crop Evol. 2011, 58, 967. [Google Scholar] [CrossRef]
  77. Laidò, G.; Mangini, G.; Taranto, F.; Gadaleta, A.; Blanco, A.; Cattivelli, L.; Marone, D.; Mastrangelo, A.M.; Papa, R.; De Vita, P. Genetic Diversity and Population Structure of Tetraploid Wheats (Triticum turgidum L.) Estimated by SSR, DArT and Pedigree Data. PLoS ONE 2013, 8, e67280. [Google Scholar] [CrossRef] [Green Version]
  78. Papi, R.M.; Spanos, K.A.; Kyriakidis, D.A. Genetic variation of Fraxinus angustifolia natural populations in Greece based on nuclear and chloroplast microsatellite markers. Eur. J. For. Res. 2012, 131, 1151–1161. [Google Scholar] [CrossRef]
  79. Fernandez-Manjarres, J.F.; Gerard, P.R.; Dufour, J.; Raquin, C.; Frascaria-Lacoste, N. Differential patterns of morphological and molecular hybridization between Fraxinus excelsior L. and Fraxinus angustifolia Vahl (Oleaceae) in eastern and western France. Mol. Ecol. 2006, 15, 3245–3257. [Google Scholar] [CrossRef]
  80. Gerard, P.R.; Fernandez-Manjarres, J.F.; Frascaria-Lacoste, N. Temporal cline in a hybrid zone population between Fraxinus excelsior L. and Fraxinus angustifolia Vahl. Mol. Ecol. 2006, 15, 3655–3667. [Google Scholar] [CrossRef] [PubMed]
  81. Hinsinger, D.D.; Basak, J.; Gaudeul, M.; Cruaud, C.; Bertolino, P.; Frascaria-Lacoste, N.; Bousquet, J. The Phylogeny and Biogeographic History of Ashes (Fraxinus, Oleaceae) Highlight the Roles of Migration and Vicariance in the Diversification of Temperate Trees. PLoS ONE 2013, 8, e80431. [Google Scholar] [CrossRef] [PubMed]
  82. Ilardi, V.; Raimondo, F.M. The genus Fraxinus, L. (Oleaceae) in Sicily. Flora Mediterr. 1999, 9, 305–318. [Google Scholar]
  83. Schicchi, R.; Marino, P. Taxa relitti della flora forestale siciliana e problemi di conservazione. Relict taxa of the Sicilian forest flora and conservation issues. Biogeographia 2011, 30, 141–150. [Google Scholar]
  84. Schicchi, R.; Camarda, L.; Di Stefano, V.; Spadaro, V.; Pitonzo, R. Analisi qualitativa dei costituenti cumarinici presenti in campioni di manna prodotti da esemplari di Fraxinus angustifolia (Oleaceae) delle Madonie. In Proceedings of the Atti Del 102 Congresso Della Societa Botanica Italiana, Palermo, Italy, 26–29 September 2007; p. 388. [Google Scholar]
  85. Minà Palumbo, F. Notizie sui frassini di Sicilia e sulla coltivazione dell’Amolleo in Castelbuono. Stamp. Leg. F. Ruffino Palermo 1847, 17. [Google Scholar]
  86. Donoghue, M.J.; Bell, C.D.; Li, J. Phylogenetic Patterns in Northern Hemisphere Plant Geography. Int. J. Plant Sci. 2001, 162, 41–52. [Google Scholar] [CrossRef] [Green Version]
  87. Magri, D.; Fineschi, S.; Bellarosa, R.; Buonamici, A.; Sebastiani, F.; Schirone, B.; Simeone, M.C.; Vendramin, G.G. The distribution of Quercus suber chloroplast haplotypes matches the palaeogeographical history of the western Mediterranean. Mol. Ecol. 2007, 16, 5259–5266. [Google Scholar] [CrossRef]
  88. Hayes, A.; Kucera, M.; Kallel, N.; Sbaffi, L.; Rohling, E.J. Glacial Mediterranean sea surface temperatures based on planktonic foraminiferal assemblages. Quat. Sci. Rev. 2005, 24, 999–1016. [Google Scholar] [CrossRef]
Plants 09 01035 g001 550
Figure 1. Genetic relationship developed using the profiles obtained from eleven nSSR (Table S2) among studied local varieties (34 samples) collected in Sicily, belonging to the manna ash germplasm. Four genotypes belonging to F. ornus were used as references. The dendrogram was developed using the UPGMA and Bruvo’s distance [51].
Figure 1. Genetic relationship developed using the profiles obtained from eleven nSSR (Table S2) among studied local varieties (34 samples) collected in Sicily, belonging to the manna ash germplasm. Four genotypes belonging to F. ornus were used as references. The dendrogram was developed using the UPGMA and Bruvo’s distance [51].
Plants 09 01035 g001
Plants 09 01035 g002 550
Figure 2. Genetic relationships among Fraxinus spp. accessions-based UPGMA and Bruvo’s distance, developed using unique nSSR profiles of sample belonging to set #2, including F. angustifolia (FAN), Fraxinus excelsior (FEX), and F. angustifolia x F. excelsior (HYB). F. ornus (FOR) was used as outgroup. Manna ash genetic profiles collected in the South of Italy are highlighted (in pink) in the phylogenetic tree.
Figure 2. Genetic relationships among Fraxinus spp. accessions-based UPGMA and Bruvo’s distance, developed using unique nSSR profiles of sample belonging to set #2, including F. angustifolia (FAN), Fraxinus excelsior (FEX), and F. angustifolia x F. excelsior (HYB). F. ornus (FOR) was used as outgroup. Manna ash genetic profiles collected in the South of Italy are highlighted (in pink) in the phylogenetic tree.
Plants 09 01035 g002
Plants 09 01035 g003 550
Figure 3. Neighbor-joining (NJ) tree based on population pairwise fixation index. Genetic distances were computed among populations grouped based on sampling locations.
Figure 3. Neighbor-joining (NJ) tree based on population pairwise fixation index. Genetic distances were computed among populations grouped based on sampling locations.
Plants 09 01035 g003
Plants 09 01035 g004 550
Figure 4. DAPC clustering of European germplasm of F. angustifolia studied, using the first two principal components (Y-axis and X-axis, respectively). The samples are grouped in five main groups: Balkans (blue; Croatia, Macedonia, Montenegro, Serbia, and Turkey), Eastern Europe (cyan; Bulgaria, Hungary, and Ukraine), France (orange), Italy (green) and Portugal (pink).
Figure 4. DAPC clustering of European germplasm of F. angustifolia studied, using the first two principal components (Y-axis and X-axis, respectively). The samples are grouped in five main groups: Balkans (blue; Croatia, Macedonia, Montenegro, Serbia, and Turkey), Eastern Europe (cyan; Bulgaria, Hungary, and Ukraine), France (orange), Italy (green) and Portugal (pink).
Plants 09 01035 g004
Table
Table 1. Genome sizes and morphological traits of studied samples, belonging to manna ash collection. F. ornus was used as reference. In bracket the number of samples analyzed belonging to each local variety/species. Three replicates for each trait and the genome sizes evaluation were analyzed.
Table 1. Genome sizes and morphological traits of studied samples, belonging to manna ash collection. F. ornus was used as reference. In bracket the number of samples analyzed belonging to each local variety/species. Three replicates for each trait and the genome sizes evaluation were analyzed.
TypeLocal VarietiesPloidy Level2C DNA Value *Apical Leaf
(Length/Width Ratio) *		Samara Stalk Length (cm) *Number of Samaras/Raceme *Flowering TimeApical Buds Colour
Manna ashAbbassa cappeddu (3)2n1.540 ± 0.010.21 ± 0.010.81 ± 0.075.51 ± 0.20November–JanuaryRed
Baciciu (4)2n1.544 ± 0.030.42 ± 0.021.12 ± 0.073.50 ± 1.02November–JanuaryRed
Cavolo (3)2n1.542 ± 0.020.23 ± 0.092.11 ± 0.065.50 ± 0.07November–JanuaryRed
Macigna (3)2n1.541 ± 0.010.42 ± 0.030.79 ± 0.026.01 ± 0.70November–JanuaryRed
Nivuru (3)2n1.541 ± 0.040.35 ± 0.013.04 ± 0.017.10 ± 0.62November–JanuaryRed
Nsiriddu (3)2n1.544 ± 0.030.24 ± 0.081.15 ± 0.055.09 ± 0.07November–JanuaryRed
Russu (3)2n1.542 ± 0.040.32 ± 0.070.68 ± 0.075.52 ± 0.27November–JanuaryRed
Sarvaggio (3)2n1.539 ± 0.020.31 ± 0.050.77 ± 0.025.01 ± 0.19November–JanuaryRed
Verdello (7)2n1.542 ± 0.050.21 ± 0.010.76 ± 0.086.53 ± 0.35November–JanuaryRed
Frassino monumentale (1)2n1.541 ± 0.010.23 ± 0.030.92 ± 0.037.05 ± 0.10November–JanuaryRed
Nsiriddu monumentale (1)2n1.544 ± 0.010.22 ± 0.010.91 ± 0.057.03 ± 0.32November–JanuaryRed
mean-1.542 **0.28 **1.18 **5.80 **--
F. ornus (4) 2n1.98 ± 0.010.52 ± 0.020.41 ± 0.0346.02 ± 2.05May–JuneWhite
* Mean values. ** Significantly different at the 0.01 probability level between local varieties and F. ornus.
Table
Table 2. Haplotypes detected based on fragment length polymorphism using six chloroplast microsatellites (cpSSR) and three plastid DNA regions in the germplasm belonging to the studied manna ash collection. F. ornus was used as reference. In bracket the number of samples analyzed belonging to each local variety/species.
Table 2. Haplotypes detected based on fragment length polymorphism using six chloroplast microsatellites (cpSSR) and three plastid DNA regions in the germplasm belonging to the studied manna ash collection. F. ornus was used as reference. In bracket the number of samples analyzed belonging to each local variety/species.
Samples/Local VarietiesNh #ccmp2ccmp3ccmp4ccmp6ccmp7ccmp10CPFRAX6atpB/rbcLmatKHaplotypes *
Abbassa cappeddu (3)11949714098117104365157253H10
Baciciu (4)11949714098117103365157253H5
Cavolo (3)11949714098117103365157253H5
Macigna (3)11949714098117103365157253H5
Nivuru (3)11949714098117103365157253H5
Nsiriddu (3)11949714098117103366157253H5 a
Russu (3)11949714098117103365157253H5
Sarvaggio (3)11949714098117103365157253H5
Verdello (7) 1949714098117103365157253H5
31949714098117103366157253H5 a
1949714098117104365157253H10
Frassino monumentale (1)11949714098117103365157253H5
Nsiriddu monumentale (1)11949714098117103365157253H5
F. ornus (4)11909714099117106364157253H19
# Nh, number of haplotypes. * Haplotype classification following Heuertz et al. (2006) [4], without CPFRAX6, atpB/rbcL and matK profiles.a H5 sub-variation identified using also CPFRAX6, atpB/rbcL and matK profiles.
Table
Table 3. Fst values (below diagonal) and Nei (1973) genetic distances (above diagonal) evaluated through nSSR on sample set #2. Each parameter was calculated for plants belonging to F. angustifolia collected in Italy—FAN (Italy), F. angustifolia sampled across Europe—FAN, F. excelsior—FEX, and hybrids—HYB (F. angustifolia × F. excelsior).
Table 3. Fst values (below diagonal) and Nei (1973) genetic distances (above diagonal) evaluated through nSSR on sample set #2. Each parameter was calculated for plants belonging to F. angustifolia collected in Italy—FAN (Italy), F. angustifolia sampled across Europe—FAN, F. excelsior—FEX, and hybrids—HYB (F. angustifolia × F. excelsior).
Group.FAN (Italy)FANHYBFEX
FAN (Italy)0.0000.2840.5360.874
FAN0.0660.0000.1590.437
HYB0.1070.0300.0000.110
FEX0.1630.0840.0280.000
Table
Table 4. Summary of genetic variation statistics at 11 nSSR loci on FAN samples belonging to set #2. Individuals were grouped based on sampling location (see Table S2).
Table 4. Summary of genetic variation statistics at 11 nSSR loci on FAN samples belonging to set #2. Individuals were grouped based on sampling location (see Table S2).
Group ID.n.IHoHeFisAR
Bulgaria80.9640.6150.525−0.2082.73
Croatia181.1560.5910.563−0.0253.05
Croatia281.0000.6140.523−0.1352.71
France171.2590.6450.632−0.0303.32
France271.3200.8030.680−0.216 *3.42
France381.3160.6140.6580.0393.32
France481.1710.6590.607−0.0743.03
France581.0940.4890.5720.204 **2.93
France681.2560.6480.626−0.0423.22
France780.9530.6590.513−0.2692.63
Hungary70.8010.8050.506−0.607 ***2.28
Italy1161.1700.5910.5530.040 ***2.96
Italy281.0320.6230.541−0.112 ***2.85
Macedonia81.3250.7500.651−0.1523.39
Montenegro81.2150.6590.607−0.0873.13
Portugal161.1850.6210.6240.0173.17
Portugal281.0290.5340.5290.0382.86
Serbia181.3230.6230.623−0.0223.40
Serbia261.1930.6670.580−0.1593.26
Turkey31.0890.7270.601−0.2413.55
Ukraine81.0400.6100.553−0.1092.88
n. = number of samples for each group; I = Shannon’s index; Ho = observed heterozygosity; He = expected; Fis = inbreeding coefficient; AR = allelic richness; * p < 0.05; ** p < 0.01; *** p < 0.001.

Share and Cite

MDPI and ACS Style

Abbate, L.; Mercati, F.; Di Noto, G.; Heuertz, M.; Carimi, F.; Fatta del Bosco, S.; Schicchi, R. Genetic Distinctiveness Highlights the Conservation Value of a Sicilian Manna Ash Germplasm Collection Assigned to Fraxinus angustifolia (Oleaceae). Plants 2020, 9, 1035. https://doi.org/10.3390/plants9081035

AMA Style

Abbate L, Mercati F, Di Noto G, Heuertz M, Carimi F, Fatta del Bosco S, Schicchi R. Genetic Distinctiveness Highlights the Conservation Value of a Sicilian Manna Ash Germplasm Collection Assigned to Fraxinus angustifolia (Oleaceae). Plants. 2020; 9(8):1035. https://doi.org/10.3390/plants9081035

Chicago/Turabian Style

Abbate, Loredana, Francesco Mercati, Giuseppe Di Noto, Myriam Heuertz, Francesco Carimi, Sergio Fatta del Bosco, and Rosario Schicchi. 2020. "Genetic Distinctiveness Highlights the Conservation Value of a Sicilian Manna Ash Germplasm Collection Assigned to Fraxinus angustifolia (Oleaceae)" Plants 9, no. 8: 1035. https://doi.org/10.3390/plants9081035

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop