DIGITALNA ARHIVA ŠUMARSKOG LISTA
prilagođeno pretraživanje po punom tekstu
|ŠUMARSKI LIST 11-12/2018 str. 53 <-- 53 --> PDF|
Fruit and seedling diversity among sweet chestnut (Castanea sativa Mill.) populations in Turkey
Raznolikost plodova i sadnica u populacijama pitomoga kestena (Castanea sativa Mill.) u Turskoj
Fahrettin Atar, Ibrahim Turna
Sweet chestnut, Castanea sativa Mill., is an important multipurpose tree species in Asia Minor and Europe. The objective of this study was to investigate variation among eight sweet chestnut populations in Turkey by using different morphological characteristics of fruits and seedlings. A total of four fruit characteristics were analysed: fruit length, width and thickness, and fruit shape, i.e. the ratio of fruit length and width. Additionally, 1000 fruit mass and fruit moisture content were determined as well. Measurements of seedling length, root collar diameter and sturdiness quotient were carried out at one-year old seedlings. The highest values of fruit length, width and thickness were found in İzmir population, while the highest values of seedling length, root collar diameter and sturdiness quotient were found in Balıkesir population. The 1000 fruit mass ranged between 3815.1 g and 10516.5 g, and the highest average fruit moisture content was 52.21 %. In general, the fruit size increased from eastern to western populations. Furthermore, the results of statistical analyses showed that there were significant differences between analysed populations for measured morphological characteristics related to both fruit and seedling. Application of cluster analysis revealed grouping of populations according to the eco-geographic principle. However, human influence on the population structure cannot be excluded as well.
Key words: Castanea sativa, sweet chestnut, Turkey, morphology, fruit, seedling
Chestnut species are an important forest trees and shrubs belonging to the Fagaceae family. The Castanea Mill. genus encompasses seven economically and ecologically significant species, widely spread in the temperate forest zone of the northern hemisphere (Johnson 1988; Lang et al. 2007), where the sweet chestnut (Castanea sativa Mill.) is the only species naturally found in Europe and Asia Minor (Kayacık 1981). Sweet chestnut is distributed across the Mediterranean region, from the Caspian Sea to the Atlantic Ocean (Fernández-López and Alía 2003). In Turkey, it can be found mainly over the North and Western Anatolia (Black Sea Coast), and the Marmara Region. Chestnut grows up to 1200 m above sea level in the Black Sea region. In addition, it can also rise up to 1700 m in Rize region and up to 1800 m in the Aegean region (Kütahya-Simav).
Naturally it forms mixture stands with other tree species (Davis 1982; Soylu 2004; Turna 2013). According to Mattioni et al. (2008) three main managing types (domestication levels) may be identified for sweet chestnut: (1) naturalized stands; (2) managed coppice; and (3) orchards.
|ŠUMARSKI LIST 11-12/2018 str. 54 <-- 54 --> PDF|
Additionally, in the Mediterranean countries there are a large number of old, grafted cultivars of sweet chestnut (Goulão et al. 2001; Pereira-Lorenzo et al. 2001, 2010; Botta et al. 2005; Martin et al. 2007; Idžojtić et al. 2012; Poljak et al. 2016, 2017), i.e. varieties of the sweet chestnut with the best quality, tasty and large fruits.
In Europe, there are three main areas (Georgia, eastern Turkey and Italy) having particular biological value for conservation of genetic resources of sweet chestnut (Villiani et al. 1999; Mattioni et al. 2017). Likewise, areas particularly rich in genetic diversity were detected in the Iberian (Martin et al. 2012) and Balkan Peninsula (Lusini et al. 2014; Poljak et al. 2017). It is important to note that some of these areas (Italy, Turkey, Iberian Peninsula) are the leading European chestnuts producers (Goulão et al. 2001). Sweet chestnut cultivars in Turkey were not accurately characterized and classified according to their origins. In addition, cultivars having the same name and different genotype emerged in many regions (Ertan 2007).
Sweet chestnut is an important multipurpose tree species used for its wood, fruit, honey, and tannin (Idžojtić et al. 2009). It is also a valuable species in ecosystems and landscapes. For example, chestnuts are rich in carbohydrates, proteins, vitamins and minerals. In addition, sweet chestnut honey has antioxidant and antimicrobial properties, and branches can be used in painting. From the perspective of the global and national forestry, sweet chestnut is of great importance with regard to versatile usage possibilities. However, chestnut forests have been seriously degraded since the introduction of chestnut diseases (Akdogan and Erkam 1968; Heiniger and Rigling 1994; Gurer 2001; Krstin et al. 2017). In addition, stand structure of chestnut forests are frequently degraded because of inappropriate silvicultural treatments (Turna et al. 2014). In studies conducted in Europe in recent years, researchers have expressed that the genetic diversity of sweet chestnut is endangered, and that it is important to ensure the conservation and sustainable use of chestnut genetic resources (Mellano et al. 2012).
In many fields of plant sciences, morphological information’s are still very important (Douaihy et al. 2012; Poljak et al. 2015) such as different taxon delimitation (Mac-Key 1988; Poljak et al. 2014a; Sękiewicz et al. 2016), population variability (Brus et al. 2011, 2016; Douaihy et al. 2012; Poljak et al. 2012, 2014a, 2018; Zebec et al. 2014, 2015), cultivar characterization (Ertan 2007; Ertan et al. 2007; Poljak et al. 2016) and selection (Polat and Özkaya 2005; Solar et al. 2001, 2005), morphological and physiological seed characterization (Powell 2010; Yilmaz and Yüksel 2014; Drvodelić et al. 2015; Daneshvar et al. 2016), and trends in leaf morphology regarding the branch position and patterns of crown plasticity (Bruschi et al. 2003; Bednorz 2006; Poljak et al. 2014b). The studies of European and Turkish sweet chestnut populations revealed high morphological variation within populations and low differentiation between populations (Villani et al. 1991; Pereira-Lorenzo et al. 1996; Serdar 1999; Podjavorsek et al. 1999; Serdar and Soylu 1999; Solar et al. 2001, 2005; Miguelez et al. 2004; Bolvanský and Užík 2005; Ertan 2007; Idžojtić et al. 2009; Mujić et al. 2010; Poljak et al. 2012). Ertan (2007) pointed out that morphological and phenological characteristics can be used to improve quantitative estimates of genetic similarities and relationships. In addition, morphological characterization is still official method for protection and registration of new cultivars (Pereira-Lorenzo et al. 1996). Moreover, information’s about the seed quality (morphological and physiological characteristics), and population diversity should be used in order to grow quality and healthy seedlings (Powell 2010).
The aim of this study was to assess variation among eight sweet chestnut populations in Turkey by using nine different morphological characteristics of fruits and seedlings.
MATERIALS AND METHODS
MATERIJALI I METODE
Chestnut fruits were collected from Adapazarı, Artvin, Aydın, Balıkesir, Bartın, İzmir, Kütahya and Sinop located in natural distribution area of Castanea sativa in Turkey (Figure 1, Table 1). An average distance of 150–200 m was established between sampled trees. Fruits were sampled from 15 to 20 trees per population.
Table 1. Coordinates and altitudes of the analysed populations.
Tablica 1 Koordinate i nadmorske visine analiziranih populacija.
After the collection, fruits from eight populations were measured in the laboratory. A total of three characteristics were measured by using a digital calliper: fruit length (FL), fruit width (FW), and fruit thickness (FT). In order to quantify the fruit shape, the ratio of fruit length and width (FL/FW) was derived. Measurements were made with millimetre (mm) sensitivity. In addition, 1000 fruit mass (1000FM)
|ŠUMARSKI LIST 11-12/2018 str. 56 <-- 56 --> PDF|
in one group, and K1, B1 and S1 populations were in another group, whereas B2, A2 and A3 populations were in the same group.
The mean values of 1000 fruit mass and fruit moisture contents related to the analysed sweet chestnut populations are shown in Table 2. The highest value for 1000 fruit mass was
|ŠUMARSKI LIST 11-12/2018 str. 57 <-- 57 --> PDF|
determined in İzmir population (10516.5 g), and the lowest value in Artvin population (3815.1 g). The highest fruit moisture content was recorded in the Sinop population (52.21 %), and the lowest in the Artvin population (38.46 %).
The cluster analysis was conducted in order to determine degree of similarity or dissimilarity among populations with regard to the fruit and seedling morphological characteristics (Figure 4). The first group was made of the İzmir and Aydın populations. Balıkesir population took place in the second group with Kütahya population. The populations from the northern region of Turkey were in third group. Furthermore, discriminant analysis was used to find out the variables which best discriminate the groups obtained by cluster analysis (I1-A1; K1-B1; B2-S1-A2-A3). The results of the discriminant analysis suggested that the diﬀerentiation between the analysed groups is significant (P<0.05). The following variables had the highest discrimination power between researched groups: FL (P=0.000), 1000FM (P=0.000), FT (P=0.001) and FW (P=0.012) exhibited the
|ŠUMARSKI LIST 11-12/2018 str. 55 <-- 55 --> PDF|
were calculated based on ISTA rules (ISTA 1993) - 800 (8×100) fruits were collected randomly from eight populations and weighed using a precision balance.
Fruit moisture content (FM) (%) was determined on a fresh mass basis using four replicates of 50 g each; fruits were weighed, oven dried at 103±1°C for 16±1 h, and reweighed (ISTA 1993).
After the measurements, fruits were sown, using a randomised sampling design, in nursery seedbeds in October. Seedling length (SdL), root collar diameter (RCD) and sturdiness quotient (SQ) were carried out at 1-year-old seedlings grown in seedbed. Measurements were made on total of 720 seedlings to be 3×30 seedlings from each populations. The sturdiness quotient refers to the ratio of the height of the seedling to the root collar diameter and expresses the vigour and robustness of the seedling (Thompson 1985; Aldhous 1994; Jaenicke 1999).
Finally, data were analysed using the SPSS 23.0 statistical program. The conducted analyses included ANOVA, Duncan’s Test, Pearson’s correlation coefficient, hierarchical cluster analysis, and discriminant analysis.
The highest values of FL, FW and FT were obtained in İzmir population. While the highest FL/FW ratio was recorded in Aydın population. Balıkesir population was characterized by the highest values of SdL, RCD and SQ. The values of fruit length ranged from 21.56 to 31.21 mm, and the mean length was 25.96 mm in all analysed populations. The fruit width in all populations ranged from 22.92 to 32.43 mm, with a mean value of 27.75 mm. The fruit thickness ranged from 14.74 to 18.99 mm, and the mean value of fruit thickness was 16.51 mm. The fruit length/width ratio varied between 0.83 and 0.98 for all populations. Average seedling length, root collar diameter and sturdiness quotient were detected to vary between 10.32-19.17 cm, 4.61-6.94 mm and 1.85-3.20, respectively. The mean values, standard deviations, maximum and minimum values of the fruit and seedling sizes are presented in Figure 2. The coefficients of variation for the studied characteristics ranged from 7.17 % to 54.04 % (Figure 3).
The ANOVA revealed that there are statistically significant differences (P<0,05) among the analysed populations in terms of all measured morphological characters. In addition, Duncan’s test was performed. For the variables: fruit width (I1-A1; K1-B1; A3-A2; B2; S1), fruit length/fruit width ratio (I1-A1-K1-A3; B1; B2; S1; A2), and the root collar diameter (B1; A3-S1; A1; I1-B2-A2; K1) five groups were revelled. Furthermore, fruit (I1-A1; K1-B1; B2-S1; A2-A3) and seedling length (K1-B2-S1-A3; I1-A1; B1; A2), as well the sturdiness quotient (B1-A2-K1; S1-B2; I1-A3; A1) formed four groups. When the groups with regard to the fruit thickness were examined: I1 and A1 populations were
|ŠUMARSKI LIST 11-12/2018 str. 58 <-- 58 --> PDF|
best distinguish, respectively. The spatial distribution of these three groups is presented in Figure 1.
Relationships among all morphological characteristics were expressed in a correlation matrix in Table 3. Accordingly, it was determined that there was statistically significant positive correlation at the 99% confidence level between fruit length, fruit width, fruit thickness and 1000 fruit mass, and at the 95% confidence level between seedling length and sturdiness quotient.
DISCUSSION AND CONCLUSIONS
RASPRAVA I ZAKLJUČCI
In this study we analysed fruit length, width, and thickness, fruit length/width ratio, 1000 fruit mass, fruit moisture content, seedling length, root collar diameter and sturdiness quotient in eight sweet chestnut populations from different regions of Turkey.
Fruit characteristics observed in this study were similar to those previously reported for the sweet chestnut populations from the following countries: Bosnia and Hercegovina, Croatia, Slovakia, Slovenia and Turkey. Mujić et al. (2010) analysed fruit morphometric characteristics in four populations in Bosnia-Herzegovina. Authors reported the following morphological characteristics: fruit length (20.62-24.70 mm), width (22.11-27.01 mm) and thickness (23.60-26.80 mm). Furthermore, Idžojtić et al. (2009) and Poljak et al. (2012) researched morphological variation of sweet chestnut populations from Croatia, and revealed high degree of morphological variability. The highest values for fruit length, width and thickness were reported for the Mediterranean and North-Western Croatian populations. In a study conducted in Slovenia on phenotypic and genotypic diversity of sweet chestnut, Solar et al. (2005) stated that the average length, width and thickness of fruits obtained from 244 trees was 27 mm, 39 mm and 19 mm, respectively. Additionally, Solar et al. (2001) compared morphological characteristics of fruits obtained from sweet chestnut populations located in three different regions in Slovenia. Authors determined the following ranges: fruit length (2.5-3.0 cm), fruit width (2.7-3.4 cm), fruit thickness (1.9-2.0 cm,), and number of fruits per kilogram (85-152). From the established variables conclusions about the fruit shape can be made. It was reported that the nut width is larger than nut height in the majority of Croatian (Idžojtić et al. 2009; Poljak et al. 2012), Slovenian (Solar et al. 2001, 2005), Slovakian (Bolvanský and Užík 2005), Bosnian Herzegovinian (Mujić et al. 2010), and Turkish (Villani et al. 1991) populations. Likewise, we found out that fruit length/width ratio for Turkish sweet chestnut populations varied between 0.8 and 0.9. Ertan et al. (2007) determined high-yielding and good-quality chestnut genotypes within naturally grown sweet chestnut populations located in Nazilli district, Aydın province. Fruit samples were collected from 80 trees, and the following values for the fruit width, length and height were observed: 18.95-23.70 mm; 35.17-41.18 mm and 30.39-34.31 mm, respectively. Similar results were reported by Ertan (2007) were fruit samples were collected from 10 sweet chestnut accessions from 10 different areas, which were selected among 80 accessions at the end of a selection study for high nut quality and high yield among natural populations in the Nazilli district. In addition, in the same study leaf morphological and fruit chemical analysis were studied as well.
The mean mass of chestnut fruits from four populations in Bosnia-Herzegovina was 4.42-6.47 g (Mujić et al. 2010). The average nut mass for Croatian populations was 7.1 g and 8.3 g (Idžojtić et al. 2009; Poljak et al. 2012). According to Ertan et al. (2007), chestnut fruits grown in Aydın-Nazilli ranged from 13.45 g to 19.96 g. The average fruit mass values for Slovenian populations ranged between 7.1 and 14.3 g (Solar et al. 2001, 2005). Serdar and Soylu (1999) pointed out that the mean mass values of fruits from the Samsun vicinity in Turkey varied between 5.3 and 15.1 g. In addition, the mass of the nuts from six natural sweet chestnut Turkish populations varied from 3.4 to 5.2. g (Villani et al. 1991). Similarly, 1000 fruit mass in our study ranged from 3815.1 g (fruit mass 3.81 g) to 10516.5 g (fruit mass 10.52 g). Chestnut forests in Turkey have a high degree of variation. In general, in our study the smaller nut mass values were observed in natural populations with undegraded stand structure. Furthermore, decrease in fruit sizes from west to east was also confirmed.
The multivariate statistical methods revelled that the populations with similar ecological conditions and being close to each other were in the same group. Solar et al. (2005) and Poljak et al. (2012) stated that sweet chestnut populations are well adapted to the climatic and soil conditions, but they
|ŠUMARSKI LIST 11-12/2018 str. 59 <-- 59 --> PDF|
differ in numerous morphological traits, productivity, and fruit quality. In addition, almost all of the populations in the third group are of natural structure. The mentioned populations, from the North Anatolia Region (Black Sea Coast) of Turkey, are in general characterized with higher genetic (Villani et al. 1999; Mattioni et al. 2017) and morphological variation. Populations in the first and second group are both natural and grafted.
Miguelez et al. (2004) found that moisture contents were over 50% in chestnut seeds obtained from 15 different populations spread over Galicia region in Spain. In our study, the fruit moisture content ranged from 38.46% to 52.21%. Differences between these two studies are probably the result of different methodologies. In our research, whole fruits were used, while Miguelez et al. (2004) analysed only the edible part of the fruit, i.e. the kernel.
In our research, sturdiness quotient ranged from 1.85 to 3.20. Sturdiness quotient is a criterion commonly used for seedling quality classification (Bacon 1979; Aldhous 1994; Genç and Yahyaoglu 2007). The ideal value for a seedling to be considered as sturdy is less than six (Jaenicke 1999). Seedlings with sturdiness ratio greater than six were actually thin, tall and etiolated, while a small quotient indicates sturdy plants with a greater chance of survival, particularly on windy or dry sites (Takoutsing et al. 2013).
As a conclusion, specific east-west increase in fruit sizes in the chestnut forests of Turkey is probably the result of ecological conditions and human influence. Those findings are in the line with the result of the previously published paper by Villani et al. (1991). Authors concluded that human influence could have enhanced the genetic, morphometric, and physiological differentiation of natural western chestnut populations with respect to the central and eastern ones. In the direction of sustainable forestry principles, the stand structure of the natural sweet chestnut forests must always be protected, and applications such as grafting works can caused decreasing of genetic diversity.
Akdogan, S., E. Erkam, 1968: Dikkat Kestane Kanseri Goruldu, Tomurcuk, 1: 4–5.
Aldhous, J.R., 1994: Nursery policy and planning. Forest Nursery Pratice. (eds. J.R. Aldhous and W.L. Mason) Forestry Commission Bulletin, 111, 1-12, London, U.K.
Bacon, G.J., 1979: Seedling morphology as an indicator of planting stock quality in conifers. Paper to IUFRO Workshop on “Techniques for Evaluating Planting Stock Quality”, New Zeland.
Bednorz, L., 2006: Morphological variability of leaves of Sorbus torminalis (L.) Crantz in Poland, Acta Soc Bot Pol, 75 (3): 233–243.
Bolvanský, M., M. Užík, 2005: Morphometric variation and differentiation of European chestnut (Castanea sativa) in Slovakia, Biologia (Bratislava), 60 (4): 423–429.
Botta, R., A. Akkak, P. Guaraldo, G. Bounous, 2005: Genetic characterization and nut quality of chestnut cultivars from Piemonte (Italy), Acta Hortic, 693: 395–401.
Brus, R., D. Ballian, P. Zhelev, M. Pandža, M. Bobinac, J. Acevski, Y. Raftoyannis, K. Jarni, 2011: Absence of geographical structure of morphological variation in Juniperus oxycedrus L. subsp. oxycedrus in the Balkan Peninsula, Eur J For Res, 130: 657–670.
Brus, R., M. Idžojtić, K. Jarni, 2016: Morphologic variation in northern marginal Juniperus oxycedrus L. subsp. oxycedrus populations in Istria, Plant Biosyst,150 (2): 274–284.
Bruschi, P., P. Grossoni, F. Bussotti, 2003: Within- and among-tree variation in leaf morphology of Quercus petraea (Matt.) Liebl. natural populations, Trees, 17: 164–172.
Daneshvar, A., M. Tigabu, A. Karimidoost, P.C. Odén, 2016: Stimulation of germination in dormant seeds of Juniperus polycarpos by stratification and hormone treatments, New Forest, 47 (5): 751–761.
Davis, P.H., 1982: Flora of Turkey-VII, Edinburg Universty Press.
Douaihy, B., K. Sobierajska, A.K. Jasińska, K. Boratyńska, T. Ok, A. Romo, N. Machon, Y. Didukh, M.B. Dagher-Kharrat, A. Boratyński, 2012: Morphological versus molecular markers to describe variability in Juniperus excelsa subsp. excelsa (Cupressaceae), AoB Plants, pls013.
Drvodelić, D., T. Jemrić, M. Oršanić, V. Paulić, 2015: Fruits size of wild apple (Malus sylvestris /L./Mill.): impact on morphological and physiological properties of seeds, Sumar List, 139 (3-4): 145–153.
Ertan, E., 2007: Variability in leaf and fruit morphology and in fruit composition of chestnuts (Castanea sativa Mill.) in the Nazilli region of Turkey, Genetic Resources and Crop Evolution, 54: 691–699.
Ertan, E., G. Seferoğlu, G.G. Dalkılıç, F.E. Tekintaş, S. Seferoğlu, F. Babaeren, M. Önal, Z. Dalkılıç, 2007: Selection of chestnuts (Castanea sativa Mill.) grown in Nazilli District, Turkey, Turk J Agric For, 31: 115–123.
Fernández-López, J., R. Alía, 2003: Technical Guidelines for genetic conservation and use for chestnut (Castanea sativa Mill.), EUFORGEN International Plant Genetic Resources Institute, Rome.
Genç, M., Z. Yahyaoğlu, 2007: Kalite Sınıflamasında Kullanılan Özellikler ve Tespiti (Properties and Determination Used in Quality Classification), Seedling Standardization, (eds. Z. Yahyaoğlu and M. Genç), 75, pp. 355–465, Publication of Süleyman Demirel University, Isparta, Turkey.
Goulao, L., T. Valdiviesso, C. Santana, C.M. Oliveira, 2001: Comparison between phonetic characterisation using RAPD and ISSR markers and phenotypic data of cultivated chestnut (Castanea sativa Mill.). Genet Resour Crop Ev, 48(4): 329–338.
Gurer, M., M.P. Ottaviani, P. Cortesi, 2001: Genetic diversity of subpopulations of Cryphonectria parasitica in two chestnut-growing regions in Turkey, For Snow Landsc Res, 76 (3): 383–386.
Heiniger, U., D. Rigling, 1994: Biological control of chestnut blight in Europe, Annu Rev Phytopathol, 32: 581–599.
Idžojtić, M., M. Zebec, I. Poljak, J. Medak, 2009: Variation of sweet chestnut (Castanea sativa Mill.) populations in Croatia according to the morphology of fruits, Sauteria, 18: 323–333.
|ŠUMARSKI LIST 11-12/2018 str. 60 <-- 60 --> PDF|
Idžojtić, M., M. Zebec, I. Poljak, Z. Šatović, Z. Liber, 2012: Analysis of the genetic diversity of “Lovran Marron” (Castanea sativa Mill.) using microsatellite markers, Sumar List, 136 (9–10): 577–585.
ISTA, 1993: International Rules for Seed Testing. Seed Science and Technology, 21:1–288.
Jaenicke, H., 1999: Good tree nursery practices: practical guidelines for research nurseries. ICRAF, Nairobi, pp 8–15.
Johnson, G.P., 1988: Revision of Castanea sect. Balanocastanon (Fagaceae). J Arnold Arboretum 69: 25–49.
Kayacık, H., 1981: Orman ve Park Ağaçlandırma Özel Sistematiği (Special System of Forest and Park Trees), Angiosperma II. Volume, İstanbul University, Faculty of Forestry Publication, No:2766/287, İstanbul.
Krstin, Lj., Z. Katanić, M. Ježić, I. Poljak, L. Nuskern, I. Matković, M. Idžojtić, M. Ćurković-Perica, 2017: Biological control of chestnut blight in Croatia: an interaction between host sweet chestnut, its pathogen Cryphonectria parasitica and the biocontrol agent Cryphonectria hypovirus 1, Pest Manag Sci, 73 (3): 582–589.
Lang, P., F. Dane, T.L. Kubisiak, H.W. Huang, 2007: Molecular evidence for an Asian origin and a unique westward migration of species in the genus Castanea via Europe to North America, Mol Phylogenet Evol, 43: 49–59.
Lusini, I., I. Velichkov, P. Pollegioni, F. Chiocchini, G. Hinkov, T. Zlatanov, M. Cherubini, C. Mattioni, 2014: Estimating the genetic diversity and spatial structure of Bulgarian Castanea sativa populations by SSRs: implications for conservation, Conserv Genet 15: 283–293.
MacKey, J., 1988: A plant breeder’s aspect on the taxonomy of cultivated plants, Biologisches Zentralblatt, 107: 369–379.
Martín, M.A., A. Moral, L.M. Martín, J.B. Alvarez, 2007: The genetic resources of European sweet chestnut (Castanea sativa Miller) in Andalusia, Spain, Genet Resour Crop Evol, 54: 379–387.
Martín, M.A., C. Mattioni, J.R. Molina, J.B. Alvarez, M. Cherubini, M.A. Herrera, F. Villani, L.M. Martín, 2012: Landscape genetic structure of chestnut (Castanea sativa Mill.) in Spain, Tree Genet Genomes, 8: 127–136.
Mattioni, C., M. Cherubini, E. Micheli, F. Villani, G. Bucci, 2008: Role of domestication in shaping Castanea sativa genetic variation in Europe, Tree Genet Genomes, 4 (3): 563–574.
Mattioni, C., M.A. Martin, F. Chiocchini, M. Cherubini, M. Gaudet, P. Pollegioni, I. Velichkow, R. Jarman, F.M. Chambers, L. Paule, V.L. Damian, G.C. Crainic, F. Villani, 2017: Landscape genetics structure of European sweet chestnut (Castanea sativa Mill): indications for conservation priorities, Tree Genet Genomes, 13:39.
Mellano, M.G., G.L. Beccaro, D. Donno, M.D. Torello, P. Boccacci, S. Canterino, A.K. Cerutti, G. Bounous, 2012: Castanea spp. biodiversity conservation: collection and characterization of the genetic diversity of an endangered species, Genet Resour Crop Ev, 59 (8): 1727–1741.
Miguelez, J.D.L.M., M.M. Bernardez, J.M.G. Queijeiro, 2004: Composition of varieties of chestnuts from Galicia (Spain). Food Chem, 84 (3): 401–404.
Mujić, I., V. Alibabić, J. Živković, S. Jahić, S. Jokić, Z. Prgomet, Z. Tuzlak, 2010: Morphological characteristics of chestnut Castanea sativa from the area of Una-Sana Canton, Journal of Central European Agriculture, 11 (2): 185–190.
Pereira-Lorenzo, S., J. Fernandez-Lopez, J. Moreno-Gonzales, 1996: Variability and grouping of Northwestern Spanish chestnut cultivars. I. Morphological traits, J Am Soc Hortic Sci, 121:183–189.
Pereira-Lorenzo, S., A.M. Ramos-Cabrer, B. Díaz-Hernández, J. Ascasíbar Errasti, F. Sau, M. Ciordia-Ara, 2001: Spanish chestnut cultivars, Hortic Sci, 36:344–347.
Pereira-Lorenzo, S., R.M. Lourenço Costa, A.M. Ramos-Cabrer, C.A. Marques Ribeiro, M.F. Serra da Silva, G. Manzano, T. Barreneche, 2010: Variation in grafted European chestnut and hybrids by microsatellites reveals two main origins in the Iberian Peninsula, Tree Genet Genomes, 6: 701–715.
Podjavoršek, A., F. Štampar, A. Solar, F. Batic, 1999: Morphological variation in chestnut (Castanea sativa Mill.) fruits in Slovenia, Acta Hort, 494: 129–132.
Polat, A.A., M. Özkaya, 2005: Selection studies on fig in the Mediterranean region of Turkey, Pak J Bot, 37 (3): 567–574.
Poljak, I., M. Idžojtić, M. Zebec, N. Perković, 2012: The variability of European sweet chestnut (Castanea sativa Mill.) in the region of northwest Croatia according to morphology of fruits, Sumar List, 136 (9-10): 479–489.
Poljak, I., M. Idžojtić, I. Šapić, J. Vukelić, M. Zebec, 2014a. Population variability of grey (Alnus incana /L./ Moench) and black alder (A. glutinosa /L./ Gaertn.) in the Mura and Drava region according to the leaf morphology, Sumar List, 138 (1-2): 7–17.
Poljak, I., M. Idžojtić, M. Zebec, 2014b: Leaf morphology of the sweet chestnut (Castanea sativa Mill.) – a Methodological approach, Acta Hort, 1043: 211–218.
Poljak, I., D. Kajba, I. Ljubić, M. Idžojtić, 2015: Morphological variability of leaves of Sorbus domestica L. in Croatia, Acta Soc Bot Pol, 84 (2): 249–259.
Poljak, I., N. Vahčić, M. Gačić, M. Idžojtić, 2016: Morphological characterization and chemical composition of fruits of the traditional Croatian chestnut variety ‘Lovran Marron’, Food Technol Biotechnol, 54 (2): 189–199.
Poljak, I., M. Idžojtić, Z. Šatović, M. Ježić, M. Ćurković-Perica, B. Simovski, J. Acevski, Z. Liber, 2017: Genetic diversity of the sweet chestnut (Castanea sativa Mill.) in Central Europe and the western part of the Balkan Peninsula and evidence of marron genotype introgression into wild populations, Tree Genet Genomes, 13:18.
Poljak, I., M. Idžojtić, I. Šapić, P. Korijan, J. Vukelić, 2018: Diversity and structure of Croatian continental and Alpine-Dinaric populations of grey alder (Alnus incana /L./ Moench subsp. incana): Isolation by distance and environment explains phenotypic divergence, Sumar List, 142 (1-2): 35–48.
Powell, A.A., 2010: Morphological and physiological characteristics of seeds and their capacity to germinate and survive, Ann Bot, 105 (6): 975–976.
Sękiewicz, K., K. Boratyńska, M.B. Dagher-Kharrat, T. Ok, A. Boratyński, 2016: Taxonomic differentiation of Cupressus sempervirens and C. atlantica based on morphometric evidence, Syst Biodivers, 14 (5): 494–508.
Serdar, U., 1999: Selection of chestnuts (Castanea sativa Mill.) in Sinop vicinity, Acta Hort, 494: 327–332.
Serdar, U., A. Soylu, 1999: Selection of chestnuts (Cestanea sativa Mill.) in Samsun vicinity, Acta Hort, 494: 333–338.
Solar, A., A. Podjavoršek, G. Osterc, F. Štapmar, 2001: Evaluation and comparison of domestic chestnut (Castanea sativa Mill.)
|ŠUMARSKI LIST 11-12/2018 str. 61 <-- 61 --> PDF|
populations in Slovenia, Forest Snow and Landscape Research, 76 (3): 455–459.
Solar, A., A. Podjavoršek, F. Štampar, 2005: Phenotypic and genotypic diversity of European chestnut (Cestanea sativa Mill.) in Slovenia-opportunity for genetic improvement. Genet Resour Crop Ev, 52: 381–394.
Soylu, A., 2004: Kestane Yetiştiriciliği ve Özellikleri, Hasad Yayıncılık, İstanbul.
Takoutsing, B., Z. Tchoundjeu, A. Degrande, E. Asaah, F.N. Gyau, A. Tsobeng, 2013: Assessing the quality of seedlings in small-scale nurseries in the Highlands of Cameroon: the use of growth characteristics and quality thresholds as indicators, Small-Scale For, 13 (1): 65–77.
Thompson, B.E., 1985: Seedling morphological evaluation- What you can tell by looking. Evaluating seedling quality: Principles, procedures, and predictive abilities of major tests, M.L. Duryea (ed.), Forest Research Laboratory, Oregon State University, Corvallis, OR, 59-71.
Turna, İ., 2013: Türkiye’de Kestane Ormanlarının Silvikültürü (silviculture of chestnut forests in Turkey), Giresun Regional Directorate, Presentation of Silviculture Education Seminar.
Turna İ., F. Atar, E. Atar, 2014: Important of chestnut (Castanea sativa Mill.) as non-wood forest products in forestry of Turkey, 3rd International Non-wood Forest Products Symposium, Turkey, pp. 958–967.
Villani, F., M. Pigliucci, M. Lauteri, M. Cherubini, 1991: Congruence between genetic, morphometric, and physiological data on differentiation of Turkish chestnut (Castanea sativa), Genome, 35: 251–256.
Villani, F., M. Lauteri, A. Sansotta, M. Cherubini, M.C. Monteverdi, C. Mattioni, 1999: Genetic structure and quantitative traits variation in F1 full-sibs progenies of Castanea sativa Mill. Acta Hort, 494: 395–405.
Zebec, M., M. Idžojtić, I. Poljak, 2014: Morphological variability of the field elm (Ulmus minor Mill. sensu latissimo) in continental Croatia, Sumar List, 138 (11-12): 563–572.
Zebec, M., M. Idžojtić, I. Poljak, I. Modrić, 2015: Population variability of wych elm (Ulmus glabra Huds.) in the mountainous region of Croatia according to the leaf morphology, Sumar List, 139 (9-10): 429–439.
Yilmaz, M., T. Yüksel, 2014: Morphological and physiological seed characteristics of Taurus fır (Abies cilicica /Ant. et Kotschy/ Carriére) in Turkey, Sumar List, 138 (11-12): 583–592.
Pitomi kesten, Castanea sativa Mill., plemenita je vrsta drveća od koje imamo višestruku gospodarsku korist (kvalitetno drvo, jestivi plodovi, med, ogrijev, listinac i dr.). Rasprostranjen je u mediteranskom području, od Kaspijskog jezera do Atlantskog oceana. U Turskoj najveće površine pod kestenovim šumama nalazimo na području sjeverne i zapadne Antolije te u regiji Marmara. U posljednjih nekoliko desetljeća pitomi kesten je ugrožen od raka kestenove kore i negativnih antropogenih utjecaja. S obzirom na to provedena su brojna istraživanja s ciljem očuvanje genofonda ove plemenite vrste drveća.
Glavni cilj ovoga istraživanja bio je utvrditi morfološku varijabilnost plodova i jednogodišnjih sadnica pitomoga kestena u Turskoj. Plodovi za morfometrijsku analizu skupljeni su tijekom listopada u osam populacija pitomoga kestena na području istočne, središnje i zapadne Turske (slika 1, tablica 1). Unutar svake populacije sakupljeni su uzorci sa po 15 do 20 stabala. Ukupno su određene po četiri značajke na svakom plodu: dužina, širina i debljina ploda te omjer dužine i širine ploda. Osim toga, određen je i udio vlage u plodovima, kao i masa 1000 zračno suhih plodova. Plodovi su u proljeće posijani na unaprijed pripremljene gredice. Na kraju prvog vegetacijskog razdoblja mjerene su sljedeće značajke: visina sadnice, promjer sadnice pri osnovi i koeficijent čvrstoće. Za utvrđivanje varijabilnosti populacija korištene su deskriptivne i multivarijatne statističke metode. Podaci su obrađeni u programskom paketu SPSS 23.0.
Rezultati deskriptivne statističke analize prikazani su na slici 2. Najviše vrijednosti za dužinu, širinu i debljinu ploda utvrđene su u populaciji Izmira, dok su najviše prosječne vrijednosti za visinu sadnice, promjer sadnice pri njenoj osnovi i koeficijent čvrstoće utvrđene u populaciji Balikesira. Masa 1000 zračno suhih plodova kretala se je od 3815,1 g do 10516,5 g, a udio vlage u plodovima od 38.46 % do 52,21 % (tablica 2). Istraživanjem je utvrđen visok stupanj varijabilnosti populacija pitomoga kestena u Turskoj (slika 3). Rezultati provedene analize varijance pokazali su da se populacije međusobno signifikantno razlikuju za sve istraživane značajke. Pearsonovim koeficijentom korelacije utvrđena je statistički značajna korelacija između dužine, širine i debljine ploda, kao i mase 1000 zračno suhih plodova (tablica 3). Osim toga, pozitivna korelacija utvrđena je i između visine sadnice i koeficijenta čvrstoće. Duncanovim testom i hijerarhijskom klasterskom analizom utvrđeno je da se one populacije koje su geografski bliže i ekološki sličnije nalaze u istoj skupini (slika 1 i 4). Također je utvrđeno da se veličina plodova u kestenovim šumama Turske povećava od istoka prema zapadu.
Ključne riječi: Castanea sativa, pitomi kesten, Turska, morfologija, plodovi, sadnice