Plant genetic resources include cultivars, landraces, unnamed genotypes, accessions, wild species closely related to cultivated varieties, breeder’s elite lines and mutants. The loss of genetic diversity caused by the practice of agriculture and the availability of genetic information has resulted in a great effort dedicated to the study and collection of plant genetic resources (Kafkas et al., 2008; Ercisli et al., 2011; Van et al., 2011; Zia-Ul-Haq et al., 2014; Eyduran et al., 2015; Akin et al., 2016).
In the last 30 years, the importance of plant genetic resources has become more evident as a result of growing concer ns about biodiversity, conservation and genetic erosion. Global food production and food security are still a major challenge for the future of mankind. Therefore, securing plant genetic resources for future generations has become a priority not only in developing countries but also throughout the world (Sahin et al., 2002; Altindag et al., 2006; Gepts, 2006; Ercisli et al., 2008; Kafkas et al., 2018).
The characterisation of fruit genetic resources by analysing plant morphology is the simplest and easiest approach (Ercisli et al., 2012: Butiuc-Keul et al., 2019; Fazenda et al., 2019). Because morphological markers, such as growth habit, fruit and seed colour, fruit and seed weight, fruit and seed shape, harvest dates, taste, plant height, disease response, and so on, are scored visually. All those traits are generally scored quickly, simply and without laboratory equipment (Bhat et al., 2010).
Three phytogeographical regions, such as Euro-Siberian, Mediterranean and Irano-Turanian, overlap in Turkey. Euro-Siberian region stretches along most of North Anatolia and Europe. Historically, Turkey has been a pathway for many civilisations and hosted many of them. The movement of communities has contributed to the enrichment of genetic diversity by transferring mainly the cultivated species and the seeds of wild plants from one place to another (Ercisli, 2004; Halasz et al., 2010). The topography of Turkey exhibits significant variety where ecological factors change frequently over a short distance. Asian section is a large, roughly rectangular peninsula situated like a bridge between Europe and Asia.
Carob tree (
The main carob producer in the world is Spain followed by Italy, Portugal, Greece, Morocco and Turkey. Turkey shares approximately 10% of the carob production in the world (FAO, 2018). Turkey has a rich natural carob population obtained from seeds, and trees thrive together with several other species of the maquis in the Mediterranean and Aegean regions. Carob has been a neglected species and accepted forest tree in Turkey. The country does not have commercial carob orchards, although some new ones have recently been established. Wild carob trees show great diversity and concentrate along the Mediterranean and Aegean regions (Figure 1) (Pazir and Alper, 2018; Durmaz and Ozel, 2019).
In Turkey, particularly in the Aegean region, carob production is still carried out using seed-propagated genotypes. Thus, in the market, carob fruits are composed of very mixed trees. Therefore, carob industry and consumers experience certain difficulties in obtaining products of standard quality. It is necessary to conduct further breeding studies using different seed-propagated carob trees and select them to increase yield and quality. The success of a breeding programme depends mainly on sound information about the breeding material.
To our knowledge, no studies are reporting morphological and biochemical analysis of seed-propagated carobs grown in the Aegean region of Turkey. Therefore, this study aimed to characterise and evaluate the diversity of 36 seed-propagated carob genotypes and develop strategies for preserving the endangered genetic resources of this species.
A total of 36 seed-propagated wild-grown carob genotypes were used, and mature pods were collected from rural areas of Marmaris district between 2016 and 2017 (Figure 1). A total of 30 pods from each genotype were randomly chosen to measure the different parameters. The morphological parameters determined were tree growth habit, leaf width, leaf length, number of leaflets/leave, pod colour, pod shape, pod surface, pod weight, pod width, pod length, pod thickness, seed colour, seed shape, seed surface, seed weight and seed ratio. Quantitative measurements were done using a calliper with a precision of ±0.1 mm and an electronic balance (SCALTEC SBA33, Heiligenstadt, Germany). The dimensions of pod, seed and leaf were measured using a digital calliper. Biochemical parameters were soluble solid content (SSC), titratable acidity, vitamin C, protein and dietary fibre contents. Seed ratio was calculated using whole pod and seed weight. For chemical analysis, pulps were crushed with a blender (Philips Hr2653/90 Viva Collection Promix, The Netherlands) and then passed through a 35-mesh sieve. About 10 g of pulp was introduced with 40 ml water in a baker and homogenised in a homogeniser (IKA, Deutschland) for 5 min. SSC of samples was measured at 25 ± 0.5 °C using a refractometer (KEM, Kyoto, Japan). Titratable acidity was determined by titration with 0.1 N NaOH and calculated as % citric acid (anhydrous) (AOAC, 2007). Vitamin C was determined by RQFlex (Merc Co, Darmstadt, Germany). Total nitrogen of carob powder was determined according to the AOAC official method and was converted to protein content using the conversion factor 6.25 (AOAC, 2007) with Macro Kjeldahl digestion and distillation apparatus. For dietary fibre analysis, 4 g of carob powder were digested with 200 ml of 5% HCL for 30 min. The mixture was filtered and washed with hot water. Then, the residue was digested with 200 ml of 5% NaOH under reflux for 30 min. The mixture was filtered and washed with distilled water until pH neutrality. The material was washed with 20 ml ethyl alcohol and 20 ml ethyl ether. Finally, the residue was dried at 100 °C for 2 h, and the residual mass was considered as fibres (De Padua et al., 2004). Protein and fibre contents were expressed as %.
No differences were found between years thus, the data of both years were pooled. All data were analysed using SPSS software and procedures. Tables of analysis of variance were constructed using the least significant difference (LSD) method at
Morphological analysis of carob leaf, pod and seed quantitative traits revealed significant variations among genotypes. Qualitative traits (colour, shape and surface aspect of pods and seeds) also showed variation among genotypes (Tables 1–3).
Tree and leaf characteristics of carob genotypes
Genotypes | Tree growth habit | Leaf width (cm) | Leaf length (cm) | Number of leaflets/leave |
---|---|---|---|---|
M1 | Open | 11.10 ab | 9.60 ab | 6.0NS |
M2 | Weeping | 8.40 e | 8.80 ab | 6.2 |
M3 | Open | 11.50 ab | 10.78 ab | 5.9 |
M4 | Open | 11.30 ab | 11.10 ab | 6.3 |
M5 | Erect | 9.85 cd | 9.40 ab | 7.0 |
M6 | Open | 9.04 de | 8.28 ab | 7.1 |
M7 | Open | 11.70 ab | 11.50 ab | 6.4 |
M8 | Open | 8.90 de | 8.82 ab | 6.3 |
M9 | Weeping | 10.42 bc | 10.30 ab | 5.9 |
M10 | Open | 9.20 d | 9.10 ab | 6.2 |
M11 | Open | 9.28 bc | 9.07 ab | 6.4 |
M12 | Open | 12.04 a | 11.60 a | 6.5 |
M13 | Erect | 9.33 cd | 9.00 ab | 7.1 |
M14 | Weeping | 11.10 b | 10.74 ab | 7.0 |
M15 | Open | 10.80 bc | 10.50 ab | 6.8 |
M16 | Open | 11.74 ab | 10.95 ab | 6.8 |
M17 | Open | 11.38 ab | 11.05 ab | 5.9 |
M18 | Weeping | 11.90 ab | 11.40 ab | 6.2 |
M19 | Open | 9.00 de | 8.04 b | 6.1 |
M20 | Open | 10.25 bc | 9.64 ab | 5.9 |
M21 | Open | 9.60 cd | 9.30 ab | 7.0 |
M22 | Weeping | 9.40 cd | 9.20 ab | 7.0 |
M23 | Open | 9.18 d | 8.80 ab | 6.5 |
M24 | Open | 10.02 cd | 9.15 ab | 6.8 |
M25 | Open | 9.56 cd | 9.28 ab | 6.8 |
M26 | Erect | 9.11 de | 9.02 ab | 6.9 |
M27 | Weeping | 10.17 c | 9.78 ab | 6.3 |
M28 | Open | 9.59 cd | 9.19 ab | 6.0 |
M29 | Open | 10.86 bc | 10.11 ab | 5.9 |
M30 | Open | 9.45 cd | 8.29 ab | 6.7 |
M31 | Open | 11.41 ab | 10.15 ab | 6.9 |
M32 | Weeping | 9.50 cd | 8.90 ab | 5.9 |
M33 | Erect | 9.33 cd | 9.02 ab | 6.4 |
M34 | Open | 10.35 bc | 10.07 ab | 6.1 |
M35 | Open | 9.20 d | 9.02 ab | 6.3 |
M36 | Open | 10.60 bc | 10.10 ab | 6.0 |
Means with different letters in the same column differ significantly (
NS, Non-significant.
Pod characteristics of carob genotypes
Genotypes | Pod colour | Pod shape | Pod surface | Pod weight (g) | Pod width (mm) | Pod length (cm) | Pod thickness (mm) |
---|---|---|---|---|---|---|---|
M1 | Dark brown | Curved | Wrinkled | 28.2 ab | 22.33 ab | 20.41 ab | 8.07 ab |
M2 | Dark brown | Spiral | Wrinkled | 12.2 cd | 14.27 d | 12.54 c | 4.82 bc |
M3 | Reddish brown | Curved | Smooth | 29.5 a | 21.67 ab | 18.94 ab | 8.11 ab |
M4 | Clear brown | Curved | Wrinkled | 25.6 ab | 22.02 ab | 17.68 b | 7.97 ab |
M5 | Reddish brown | Straight | Smooth | 15.4 cd | 17.44 c | 16.38 bc | 5.18 bc |
M6 | Dark brown | Curved | Wrinkled | 16.1 cd | 17.66 bc | 15.91 bc | 5.63 bc |
M7 | Clear brown | Curved | Smooth | 25.5 ab | 19.33 bc | 18.27 ab | 7.08 ab |
M8 | Clear brown | Curved | Smooth | 17.7 bc | 16.94 cd | 14.03 bc | 4.88 bc |
M9 | Dark brown | Spiral | Rough | 23.4 b | 21.14 ab | 13.98 bc | 5.94 bc |
M10 | Dark brown | Curved | Wrinkled | 16.6 cd | 17.76 bc | 16.47 bc | 5.56 bc |
M11 | Clear brown | Straight | Wrinkled | 15.2 cd | 19.56 bc | 16.87 nc | 6.36 bc |
M12 | Dark brown | Curved | Wrinkled | 26.3 ab | 23.08 a | 19.83 ab | 8.37 a |
M13 | Reddish brown | Curved | Smooth | 16.2 cd | 20.50 ab | 19.33 ab | 6.02 bc |
M14 | Dark brown | Straight | Wrinkled | 25.6 ab | 18.15 bc | 19.98 ab | 7.11 ab |
M15 | Reddish brown | Straight | Smooth | 22.1 bc | 19.10 bc | 18.55 ab | 6.20 bc |
M16 | Clear brown | Curved | Smooth | 25.1 ab | 22.48 ab | 20.02 ab | 8.02 ab |
M17 | Dark brown | Curved | Rough | 28.4 ab | 20.83 ab | 21.67 a | 7.92 ab |
M18 | Dark brown | Spiral | Wrinkled | 25.3 ab | 20.21 b | 20.90 ab | 7.62 ab |
M19 | Reddish brown | Curved | Wrinkled | 15.6 cd | 16.56 cd | 17.10 bc | 5.35 bc |
M20 | Reddish brown | Spiral | Smooth | 21.3 bc | 19.61 bc | 19.03 ab | 6.40 bc |
M21 | Dark brown | Curved | Wrinkled | 19.7 bc | 19.23 bc | 17.90 ab | 5.95 bc |
M22 | Clear brown | Spiral | Smooth | 17.7 bc | 18.78 bc | 19.04 ab | 6.03 bc |
M23 | Dark brown | Curved | Wrinkled | 10.9 d | 18.52 bc | 14.21 bc | 4.77 bc |
M24 | Dark brown | Curved | Smooth | 22.3 bc | 20.07 bc | 19.43 ab | 5.81 bc |
M25 | Dark brown | Straight | Smooth | 17.4 c | 18.20 bc | 16.84 bc | 5.70 bc |
M26 | Reddish brown | Straight | Wrinkled | 19.4 bc | 20.22 b | 14.98 bc | 6.35 ab |
M27 | Clear brown | Curved | Wrinkled | 21.6 bc | 18.41 bc | 18.95 ab | 6.82 ab |
M28 | Dark brown | Straight | Wrinkled | 12.6 cd | 18.10 bc | 12.88 c | 5.91 bc |
M29 | Reddish brown | Curved | Smooth | 11.4 bc | 19.07 bc | 18.23 ab | 7.30 ab |
M30 | Clear brown | Curved | Smooth | 9.2 de | 15.44 cd | 16.67 bc | 6.58 b |
M31 | Dark brown | Curved | Wrinkled | 25.5 ab | 20.18 b | 19.19 ab | 6.24 bc |
M32 | Reddish brown | Curved | Smooth | 15.0 cd | 17.60 bc | 17.94 ab | 5.59 bc |
M33 | Reddish brown | Spiral | Smooth | 10.3 de | 15.46 cd | 14.73 bc | 4.65 c |
M34 | Dark brown | Spiral | Wrinkled | 21.9 bc | 20.70 ab | 20.19 ab | 6.47 b |
M35 | Clear brown | Curved | Wrinkled | 8.3 e | 16.11 cd | 14.98 bc | 4.91 bc |
M36 | Dark brown | Curved | Wrinkled | 22.6 bc | 18.64 bc | 19.23 ab | 7.71 ab |
Means with different letters in the same column differ significantly (
Seed characteristics of carob genotypes
Genotypes | Seed colour | Seed shape | Seed surface | Total seed weight (g) | Seed ratio (%) |
---|---|---|---|---|---|
M1 | Dark brown | Rounded | Wrinkled | 3.41 a | 12.09 ab |
M2 | Dark brown | Elliptical | Smooth | 1.24f g | 10.16 ab |
M3 | Clear brown | Rounded | Smooth | 3.20 ab | 10.85 ab |
M4 | Clear brown | Rounded | Wrinkled | 3.07 ab | 11.99 ab |
M5 | Reddish brown | Oval | Smooth | 1.85 de | 12.01 ab |
M6 | Dark brown | Rounded | Wrinkled | 1.72 e | 10.68 ab |
M7 | Clear brown | Rounded | Smooth | 3.01 b | 11.80 ab |
M8 | Clear brown | Rounded | Smooth | 1.60 ef | 9.04 b |
M9 | Dark brown | Elliptical | Rough | 2.30 cd | 9.83 ab |
M10 | Dark brown | Rounded | Wrinkled | 1.57 ef | 9.46 ab |
M11 | Clear brown | Elliptical | Smooth | 1.62 ef | 10.66 ab |
M12 | Dark brown | Rounded | Very rough | 2.90 bc | 11.03 ab |
M13 | Clear brown | Oval | Smooth | 1.48 ef | 9.14 ab |
M14 | Dark brown | Elliptical | Wrinkled | 2.87 bc | 11.21 ab |
M15 | Reddish brown | Elliptical | Smooth | 2.20 cd | 9.95 ab |
M16 | Clear brown | Rounded | Smooth | 2.69 bc | 10.72 ab |
M17 | Dark brown | Rounded | Very rough | 2.55 c | 8.98 bc |
M18 | Dark brown | Elliptical | Wrinkled | 2.45 cd | 9.68 ab |
M19 | Reddish brown | Oval | Wrinkled | 1.35 f | 8.65 bc |
M20 | Clear brown | Elliptical | Smooth | 2.36 cd | 11.08 ab |
M21 | Blackish brown | Rounded | Wrinkled | 1.40 ef | 7.11 bc |
M22 | Clear brown | Oval | Smooth | 1.58 ef | 8.93 bc |
M23 | Dark brown | Rounded | Wrinkled | 1.19 fg | 10.91 ab |
M24 | Blackish brown | Rounded | Smooth | 1.98 de | 8.88 bc |
M25 | Dark brown | Elliptical | Smooth | 1.48 ef | 8.51 bc |
M26 | Reddish brown | Elliptical | Wrinkled | 1.22 fg | 6.29 c |
M27 | Clear brown | Rounded | Wrinkled | 2.15 d | 9.95 ab |
M28 | Dark brown | Oval | Wrinkled | 1.16 fg | 9.21 ab |
M29 | Clear brown | Rounded | Smooth | 2.26 cd | 10.56 ab |
M30 | Clear brown | Rounded | Smooth | 1.10 g | 11.96 ab |
M31 | Blackish brown | Rounded | Wrinkled | 2.61 bc | 10.24 ab |
M32 | Clear brown | Rounded | Smooth | 1.28 fg | 8.53 bc |
M33 | Clear brown | Elliptical | Smooth | 1.20 fg | 11.6 5 ab |
M34 | Clear brown | Elliptical | Smooth | 2.60 bc | 11.87 ab |
M35 | Clear brown | Rounded | Smooth | 1.16 fg | 13.98 a |
M36 | Blackish brown | Rounded | Smooth | 2.05 de | 9.07 b |
Means with different letters in the same column differ significantly (
The genotypes exhibited three tree growth habits, such as open, weeping and erect, and among them open growth habit was dominant followed by weeping (Table 1). Batlle and Tous (1997) reported that open growth habit was dominant among carob cultivars from Spain, Italy, Portugal, Greece, Tunisia and the USA followed by weeping growth habit.
The genotypes differed from each other statistically (
Pod characteristics (colour, shape, surface, weight, width, length and thickness) are provided in Table 2.
The majority of genotypes had dark-brown pod colour (47.22%) followed by reddish brown (27.78%) and clear brown (25.00%). Dark-brown, clear-brown and reddish-brown pod colours were previously reported in carob cultivars and genotypes (Batlle and Tous, 1997; Ait Chitt et al., 2007). Curved pod shape was dominant (61.11%) among genotypes followed by equally spiral and straight shape (19.44%). Batlle and Tous (1997) reported a curved, spiral and straight pod shape among carob cultivars and genotypes, which is in accordance with our study. In terms of pod surface, 19 genotypes had a wrinkled surface (52.78%) followed by 15 genotypes with a smooth surface (41.67%) and 2 genotypes with a rough surface (5.56%) (Table 2). Batlle and Tous (1997) reported that the pod surface varied from smooth to wrinkled in carobs.
Pod weight and pod dimensions (width, length, length and thickness) are shown in Table 2, and we found statistically significant differences among genotypes (
Pod weight of 36 carob genotypes was quite variable and ranged from 8.3 g (M35) to 29.5 g (M3) among genotypes. The average pod dimensions (width, length and thickness) were found between 14.27 and 23.38 mm, 12.54 and 21.67 cm and 4.80–8.37 mm for the wild genotypes (Table 2). La Malfa et al. (2012) investigated morphological and technological characteristics of eight carob cultivars grown in Sicily, Italy, and reported average pod weight, pod width, pod length and pod thickness as 13.7–33.4 g, 19.3–26.8 mm, 14.9–22.9 cm and 6.8–14.0 mm, respectively. In Algeria, a study examined wild-grown carobs in 10 regions and reported average pod weight, pod width, pod length and pod thickness as 7.04–30.57 g, 18.10–31.80 mm, 10.30–18.75 cm and 4.50–8.20 mm, respectively (Boublenza et al., 2019). Barracosa et al. (2007) stated pod weight, pod width, pod length and pod thickness of 15 carob cultivars from Portugal as 13.20–26.39 g; 16.16–23.38 mm; 12.95–20.35 cm and 7.19–10.86 mm, respectively. Albanell et al. (1991) reported the highest pod weight (14.88 g), pod length (15.83 cm) and pod width (21.10 mm) among 182 common carob trees from various areas in Spain. Haddarah et al. (2013) reported pod weight (8.93–36.85 g), pod length (11.42–24.25 cm), pod width (17.30–27.40 mm) and pod thickness (4.8–9.2 mm) among wild carob genotypes in Lebanon. Russo and Polignano (1996) found mean pod length and width as 17.1 cm and 22.7 mm, respectively. Gharnit et al. (2006) reported average pod length, width and thickness as 13.5 cm, 19.5 mm and 6.9 mm in Morocco. Our results are in good agreement with the aforementioned studies. The main selection criteria in carobs have traditionally focussed on large pod size, high pulp and sugar content. Carob pod size is also important to withstand strong winds during spring to prevent premature fruit drop (Batlle and Tous, 1997).
Seed colour, seed shape, seed surface, total seed weight and seed ratio are shown in Table 3. Most of the genotypes had clear-brown pod colour (44.4%) followed by dark brown (33.3%), reddish brown (11.1%) and blackish brown (11.1%). Rounded pod shape was dominant (55.5%) among genotypes followed by elliptical (30.5%) and oval seed shape (13.8%). In terms of seed surface, 55.5% of the genotypes had smooth seed surface, 36.1% of the genotypes had wrinkled surface, 5.55% of the genotypes had very rough and 2.77% of the genotypes had rough seed surface (Table 3). Albanell et al. (1991) and Batlle and Tous (1997) reported that the majority of carob seeds had a smooth seed surface.
There were statistically significant differences (
The biochemical characteristics of carob genotypes fruits are shown in Table 4. SSC, titratable acidity, protein and dietary fibre contents differed significantly among genotypes (
Biochemical characteristics of carob pods
Genotypes | SSC (%) | Acidity (%) | Vitamin C (mg ∙ 100 g−1) | Protein (%) | Dietary fibres (%) |
---|---|---|---|---|---|
M1 | 67.21 ab | 0.76 bc | 10.1NS | 3.88 bc | 7.0 b |
M2 | 53.12 d | 0.88 ab | 9.3 | 6.50 ab | 6.0 cd |
M3 | 68.41 ab | 0.60 bc | 8.3 | 4.77 bc | 7.7 a |
M4 | 65.45 ab | 0.80 bc | 9.4 | 4.59 bc | 5.8 cd |
M5 | 59.56 c | 0.68 bc | 7.6 | 5.25 bc | 5.5 de |
M6 | 57.23 cd | 0.55 bc | 9.8 | 3.73 c | 5.0 de |
M7 | 68.23 ab | 0.92 ab | 7.1 | 5.40 ab | 6.8 bc |
M8 | 54.14 cd | 0.85 b | 7.5 | 5.04 bc | 6.3 c |
M9 | 64.11 b | 1.12 a | 7.6 | 4.94 bc | 6.1 cd |
M10 | 58.28 cd | 1.02 ab | 8.0 | 3.96 bc | 5.0 de |
M11 | 57.45 cd | 1.05 ab | 6.6 | 4.11 bc | 4.9 e |
M12 | 69.36 a | 0.55 bc | 10.2 | 6.95 a | 5.3 de |
M13 | 59.98 bc | 0.45 c | 9.4 | 4.20 bc | 6.6 bc |
M14 | 67.56 ab | 0.78 bc | 8.7 | 5.35 b | 5.8 cd |
M15 | 63.44 bc | 0.83 b | 7.6 | 4.30 bc | 5.3 de |
M16 | 65.45 ab | 0.90 ab | 7.5 | 4.22 bc | 5.6 d |
M17 | 68.22 ab | 0.66 bc | 8.0 | 6.02 ab | 4.9 e |
M18 | 66.44 ab | 0.59 bc | 8.4 | 6.18 ab | 5.0 de |
M19 | 51.56 de | 0.62 bc | 5.9 | 5.44 ab | 5.3 de |
M20 | 63.30 bc | 0.75 bc | 6.2 | 5.50 ab | 7.1 ab |
M21 | 58.12 cd | 0.84 b | 5.8 | 4.33 bc | 5.4 de |
M22 | 57.64 cd | 0.90 ab | 5.9 | 5.10 bc | 5.7 cd |
M23 | 49.36 e | 1.00 ab | 7.1 | 4.60 bc | 7.0 b |
M24 | 62.55 bc | 1.05 ab | 7.7 | 4.11 bc | 5.9 cd |
M25 | 56.35 cd | 0.96 ab | 8.5 | 4.70 bc | 5.6 d |
M26 | 55.83 cd | 0.92 ab | 9.2 | 4.15 bc | 6.4 bc |
M27 | 63.13 bc | 0.71 bc | 7.4 | 6.44 ab | 7.0 b |
M28 | 52.35 de | 0.77 bc | 8.1 | 5.33 b | 6.2 cd |
M29 | 61.21 bc | 0.84 b | 7.7 | 5.30 b | 5.0 de |
M30 | 50.45 de | 0.55 bc | 6.8 | 5.04 bc | 5.5 de |
M31 | 67.40 ab | 0.80 bc | 7.3 | 4.27 bc | 7.4 ab |
M32 | 51.80 de | 0.93 ab | 6.4 | 4.41 bc | 6.4 bc |
M33 | 49.74 de | 0.76 bc | 7.7 | 4.50 bc | 6.0 cd |
M34 | 60.80 bc | 0.64 bc | 8.2 | 4.90 bc | 5.8 cd |
M35 | 49.56 de | 0.68 bc | 8.0 | 3.95 bc | 5.4 de |
M36 | 62.26 bc | 0.91 ab | 7.5 | 4.44 bc | 5.0 de |
Means with different letters in the same column differ significantly (
NS, Non-significant.
The highest SSC content was seen in genotype M12 as 69.36% followed by M3 (68.41%) and M7 (68.23%), while the lowest SSC content was obtained from M23 genotype as 49.36% (Table 4). Titratable acidity and vitamin C were less variable than SSC and ranged from 0.45% (M13) to 1.12% (M9) and from 5.9 mg ∙ 100 g−1 (M19 and M22) to 10.2 mg ∙ 100 g−1 (M12), respectively (Table 4). SSC values of carob genotypes have been reported to be between 32 and 70% (Marakis et al., 1988).
Protein and dietary fibre contents were found between 3.73% (M6) and 6.95% (M12) and 4.9% (M11 and M17) and 7.7% (M3), respectively (Table 4). Haddarah et al. (2013) reported protein content between 3.61 and 4.82% and dietary fibre content between 4.80 and 7.74% among wild carob genotypes in Lebanon. Ozcan et al. (2007) found that carob pods had 4.71% protein content and 9.69% crude fibre content.
The study showed variation among wild carob populations for leaf, pod and seed morphology. In the perspective of identifying the best genotypes for breeding programmes and/or accession collection, additional descriptors should be examined such as regular bearing (Keles and Bilir, 2015); gender and harvest period or fruit ripening (Tous et al., 2009), pedicel length as a criterion of pod abscission (Tous et al., 2009); trunk cross-section and canopy volume (Tous et al., 2009), fruit sweetness, flowering and fruiting phenology and precocity (Haddarah et al., 2013).
PCoA was applied to the data using NTSYS 2.10e software, and the contribution rates of the first three principal coordinates were 47.1, 22.4 and 9.2%, respectively, accounting for 78.7% of the variance. The first principal coordinate (PCoA1), which explains 47.1% of the overall variance, is identified with the pod weight, pulp weight and seed weight, while the second principal coordinate (PCoA2) is related to the leaf and leaflet dimensions, pod length and pulp and seed ratio (Table 5). Carob genotypes samples were partitioned into four distinct groups. PCoA Groups 1, 2, 3 and 4 included 10, 8, 10 and 8 samples, respectively (Figure 2). The first group characterised by high pod and seed weight, larger and longer leaves, high seed size and high SSC content. The second and third groups had medium-sized leaves, pods and seeds and medium sugar content. The last group had lower pod and seed weight, low leaf dimensions and low sugar content. PCoA revealed useful information on the characterisation and comparison of carob germplasm collections in terms of morphological and biochemical data. At the same time, PCoA indicated some common features of wild carob genotypes, thanks to which it is possible to divide the analysed wild carobs into bigger fruited ones, more sweet ones, or those with a higher content of pulp and seed ratio. The substantial dispersion of Turkish wild carob genotypes in the PCoA plot suggests a high level of diversity, which can make them attractive for future breeding programmes and long-term conservation strategies.
Factor loadings for each variable on the components of PCoA analysis
Variable | PC1 | PC2 | PC3 |
---|---|---|---|
Leaf length | 5.54 | 13.11 | 1.20 |
Leaf width | 1.12 | 18.74 | 1.03 |
Number of leaflets | 4.13 | 10.11 | 0.17 |
Length of leaflets | 0.03 | 16.13 | 1.67 |
Pod weight | 22.71 | 0.10 | 0.55 |
Pod width | 9.22 | 0.50 | 9.15 |
Pod length | 2.45 | 11.23 | 4.66 |
Pod thickness | 7.11 | 0.08 | 7.57 |
Pulp weight | 22.13 | 0.80 | 6.21 |
Seed weight | 10.06 | 0.57 | 14.13 |
Seed number | 7.06 | 0.09 | 25.11 |
Pulp weight | 3.41 | 2.23 | 8.62 |
Seed ratio | 1.45 | 12.09 | 15.37 |
Pulp ratio | 2.23 | 10.53 | 4.22 |
pH | 0.34 | 1.03 | 0.07 |
SSC | 0.49 | 0.90 | 0.05 |
Acidity | 0.13 | 0.56 | 0.13 |
Vitamin C | 0.04 | 0.08 | 0.00 |
Protein | 0.23 | 0.09 | 0.05 |
Dietary fibre | 0.12 | 0.03 | 0.04 |
Eigenvalue | 5.43 | 2.98 | 1.67 |
% of variance | 47.1 | 22.4 | 9.2 |
Cumulative variance | 47.1 | 69.5 | 74.7 |
Our findings showed that morphological characteristics and biochemical composition were considerably influenced by the genotype factor. Even though such variation did not seem to be geographically structured because all genotypes are from similar ecological and soil conditions, and the analysed traits could be considered under an agronomic and an industrial perspective (seed yield and pulp weight). Such descriptors, together with additional ones, would contribute to the characterisation of carob genetic resources and guide the choice of populations for