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Variation in oil content in Camellia japonica seeds

 

De Ron, A.M.1,3*, Salinero M.C.2,3, Vela, P.2,3

1 Misión Biológica de Galicia, Spanish National Research Council (CSIC), El Palacio-Salcedo, 36143 Pontevedra, Spain. * E-mail: amderon@mbg.csic.es
2 Estación Fitopatolóxica do Areeiro, Deputación de Pontevedra, Subida a la Robleda s/n, 36153 Pontevedra, Spain.
3 Associated Unit Agroforestry Systems (SA-EFA). Pontevedra, Spain

Introduction

      The genus Camellia is one of 30 included in the family Theaceae and comprises 284 species (Chang and Bartholomew, 1984), two of which have outperformed all others until a few years ago: C.sinensis, from whose leaves tea is obtained, and C. japonica, of great interest as an ornamental plant (Samartín and Pérez, 1984). Today other species are becoming important such as C. grijsii, C. longicarpa, C. maliflora, C. oleifera, C. salicifolia, C. taliensis, C. yuhsienensis and C. yunnanensis: some have been used in Asia for centuries for the production of oils used in both food and cosmetics.
      Very little data is available on the date of the introduction of the first camellias in Europe. The first living camellias documented were exhibited in England in 1739, in the greenhouses of the gardens of Robert James, 8th Lord Petre, at Thorndon Hall (Essex), and were probably brought from China by Jesuit missionaries (Samartín and Pérez, 1988) or by English merchants and sailors (Short, 2005). There are two surviving paintings of these plant; one depicting a red flower and the other a white flower.
      The genus Camellia was introduced into Galicia (NW Spain) in the XIX century (Salinero and Vela, 2003). At first it was mainly cultivated in “Pazos”- palaces - belonging to the Galician nobility, where suitable growing conditions were found: both climate and fertile soil. Currently different species of the genus Camellia (mainly C. japonica) are present in many gardens in the North and Northwest Spain adapted to a wide range of uses, although it is more common to see them as an isolated tree or in groups where various species and cultivars of different flowers give colour for long periods of time (September to May) in the garden. Many experts are surprised to see that in Galicia camellias grow splendidly despite being neglected for long periods of time, while in other regions of Spain or Europe they need constant care is, requiring even the protection of a greenhouse. In general, it is accepted that cold weather and even rain can damage the winter blooms of Camellia species, however both factors benefit growth, and interestingly in several countries, even those less favourable for Camellia cultivation, it is common to use them to form hedges and protective barriers around the edges of gardens, orchards and flower beds.
      In recent years, the number of pests and diseases detected in Camellia has increased considerably. This may be related to the widespread and increasing international trade and the exchange of plant material that has contributed to the spread of pathogens. In addition, the varie environmental conditions in which it develops can also affect the occurrence of pests and diseases (Varela et al., 2003).

      Camellia oil is considered one of the best cooking oils in the world (Huang et al., 2013). Camellia oil, extracted from different species has long been processed as industrial oil, used in the production of cosmetics, soaps, hair oil, medicines and now it is generating interest also as a biofuel source (Lin and Fan, 2011). However, today these plants are grown on a large scale in China and to a lesser extent Japan. Outside Asia, the uses and development process of this camellia oil is unknown. Camellia oil is extracted by pressing the seeds. Its composition is very similar to olive oil, both of which are very beneficial to health. Furthermore, camellia oil has a higher concentration of monounsaturated fatty acids, beneficial to health because it reduces levels of bad cholesterol. The oil can also be used cosmetically in the preparation of shampoos, soaps, creams, etc. The objective of the present work was to analyze the variation in oil content in Camellia japonica seeds from plants growing in different locations of Galicia (NW Spain).

Material and methods

      Seeds of 61 C. japonica plants from different genotypes growing in different locations were analyzed (Table 1). The traits studied were: seed weight (g), number of seeds/100 g, seed oil content (%, g) and oil density (g/ml).

Table 1. C. Japonica cultivars and locations of the seed sampling.

 Genotype Location Nr. Plants
 jap-Brava 1  Areeiro (Pontevedra, Spain)  6
 jap-Brava 2  Areeiro (Pontevedra, Spain)  6
 71 - Furo-An  Areeiro- z10 (Pontevedra, Spain)  6
 71 - Furo-An  Areeiro- z7 (Pontevedra, Spain)  5
 91 - Yosemite  Areeiro-4b (Pontevedra, Spain)  3
 108 - Shirobotan  Areeiro-I (Pontevedra, Spain)  3
 91 - Yosemite  Areeiro-III (Pontevedra, Spain)  3
 Plant 1  Lourizán (Pontevedra, Spain)  6
 Plant 2  Lourizán (Pontevedra, Spain)  6
 Plant 1  Rubiáns (Vilagarcía de Arousa, Spain)  6
 Plant 2  Rubiáns (Vilagarcía de Arousa, Spain)  6
 Plant 1  San Cibrán (Vedra, Spain)  5

 

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 1           2

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3          4

Figure 1. Sampling locations. 1: Areeiro, 2: Lourizán, 3: Rubiáns, 4: San Cibrán

 

      Samples of fruits of were collected in autumn from healthy plants in the different sampling locations. The harvest was carried out when fruits began to split open and the seeds were visible, a phenological stage of fruit development that corresponds to the BBCH stage 88 described for C. japonica (Vela et al., 2013). For each plant, a seed sample of 1 kg was taken and divided into five 200 g subsamples. Oil extraction was performed for each subsample.

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Figure 2. Pressing the seeds

phpCNXIg8Figure 3. Filtering the oil

 

Results and discussion


      Table 2 displays the results of the traits studied in the 61 C. japonica plants from several genotypes studied in different locations. The seed oil content averaged 20.8 %, with a range of variation from a minimum of 5.5 % in 91-Yosemite at Areeiro-b4 to a maximum of 29.6 % in a plant at Lourizán, which confirms the environmental effects on oil content described in C. reticulata by Huang et al. (2013). This variability in the oil content reflects phenotypic diversity that could be the basis for a selection program to improve the oil content in the C. japonica seeds. Table 3 summarizes the oil content by genotype and location, to support that hypothesis.
      The correlation between seed weight and oil content was not significant for the complete set of plants, but in the subsample of those plants (31) that were richer in total oil content (>0.200 g/seed), the correlation coefficient of -0.428 was highly significant, which means that in rich-oil seeds, seed size has a negative effect on the total oil content.

Table 2. Results of the traits studied in the 61 C. japonica plants analyzed.

 Genotype Location Seed
weight (g) 

 Number of seeds/100g

 Seed oil content (%)  Seed oil content  (g)  Oil density (g/ml)
 jap-Brava 1  Areeiro  0.589  169.8  23.7  0.139  0.879
 jap-Brava 1  Areeiro  0.578  173.0  25.8  0.149  0.871
 jap-Brava 1  Areeiro  0.473  211.6  24.5  0.116  0.912
 jap-Brava 1  Areeiro  0.579  172.7  24.2  0.140  0.899
 jap-Brava 1  Areeiro  0.716  139.7  24.1  0.173  0.908
 jap-Brava 1  Areeiro  0.646  154.8  23.2  0.150  0.914
 jap-Brava 2  Areeiro  1.195  83.7  26.9  0.321  0.912
 jap-Brava 2  Areeiro  1.149  87.1  27.3  0.313  0.909
 jap-Brava 2  Areeiro  1.248  80.1  25.9  0.324  0.914
 jap-Brava 2  Areeiro  1.280  78.1  24.1  0.309  0.923
 jap-Brava 2  Areeiro  1.238  80.8  25.1  0.311  0.905
 jap-Brava 2  Areeiro  1.155  86.6  28.1  0.324  0.891
 71 - Furo-An  Areeiro- z10  1.257  79.6  20.0  0.252  0.913
 71 - Furo-An  Areeiro- z10  1.001  99.9  21.6  0.216  0.912
 71 - Furo-An  Areeiro- z10  1.169  85.6  21.1  0.246  0.904
 71 - Furo-An  Areeiro- z10  1.291  77.5  22.6  0.291  0.905
 71 - Furo-An  Areeiro- z10  0.969  103.2  21.3  0.206  0.900
 71 - Furo-An  Areeiro- z10  1.096  91.2  21.1  0.231  0.906
 71 - Furo-An  Areeiro- z7  1.459  64.1  22.2  0.346  0.896
 71 - Furo-An  Areeiro- z7  1.161  86.1  22.9  0.266  0.896
 71 - Furo-An  Areeiro- z7  1.060  94.4  23.6  0.250  0.896
 71 - Furo-An  Areeiro- z7  1.272  78.6  24.2  0.307  0.906
 71 - Furo-An  Areeiro- z7  1.318  75.9  22.0  0.290  0.903
 91 - Yosemite  Areeiro- 4b  0.906  110.4  5.8  0.052  0.864
 91 - Yosemite  Areeiro- 4b  0.890  112.3  5.5  0.049  0.839
 91 - Yosemite  Areeiro- 4b  0.821  121.8  5.7  0.046  0.834
 108 - Shirobotan  Areeiro- l  1.122  89.1  13.4  0.150  0.879
 108 - Shirobotan  Areeiro- l  1.120  89.3  13.3  0.149  0.857
 108 - Shirobotan  Areeiro- l  1.041  96.0  13.1  0.137  0.869
 91 - Yosemite  Areeiro- lll  0.965  103.6  7.5  0.072  0.836
 91 - Yosemite  Areeiro- lll  0.747  133.9  9.1  0.068  0.847
 91 - Yosemite  Areeiro- lll  0.745  134.3  8.8  0.066  0.835
 Plant 1  Lourizán  0.823  121.6  28.3  0.233  0.898
 Plant 1  Lourizán  0.862  116.0  28.8  0.248  0.891
 Plant 1  Lourizán  0.752  133.1  28.2  0.212  0.889
 Plant 1  Lourizán  0.731  136.9  29.6  0.217  0.884
 Plant 1  Lourizán  0.921  108.6  26.4  0.243  0.890
 Plant 1  Lourizán  0.822  121.6  28.0  0.230  0.884
 Plant 2  Lourizán  0.739  135.3  26.2  0.194  0.882
 Plant 2  Lourizán  0.640  156.3  28.9  0.185  0.856
 Plant 2  Lourizán  0.705  141.8  27.4  0.193  0.875
 Plant 2  Lourizán  0.558  179.1  29.0  0.162  0.863
 Plant 2  Lourizán  0.750  133.4  29.4  0.221  0.876
 Plant 2  Lourizán  0.760  131.6  29.6  0.225  0.870
 Plant 1  Rubiáns  0.697  143.5  20.3  0.141  0.890
 Plant 1  Rubiáns  0.810  123.4  21.6  0.175  0.906
 Plant 1  Rubiáns  0.443  225.9  20.2  0.089  0.906
 Plant 1  Rubiáns  0.622  160.7  21.6  0.135  0.904
 Plant 1  Rubiáns  0.545  183.4  20.3  0.111  0.897
 Plant 1  Rubiáns  0.704  142.1  23.4  0.165  0.909
 Plant 2  Rubiáns  0.811  123.2  24.5  0.199  0.901
 Plant 2  Rubiáns  0.934  107.1  23.0  0.215  0.909
 Plant 2  Rubiáns  0.587  170.4  23.5  0.138  0.900
 Plant 2  Rubiáns  0.915  109.3  23.1  0.211  0.902
 Plant 2  Rubiáns  0.619  161.7  22.8  0.141  0.905
 Plant 2  Rubiáns  1.127  88.8  23.5  0.265  0.899
  Plant 1  San Cibrán  1.201  83.3  23.6  0.283  0.916
  Plant 1  San Cibrán  0.836  119.7  23.0  0.192  0.904
  Plant 1  San Cibrán  0.890  112.4  20.7  0.184  0.908
  Plant 1  San Cibrán  0.915  109.3  22.8  0.209  0.912
  Plant 1  San Cibrán  0.898  111.3  22.7  0.204  0.916

 

Table 3. Oil content by genotype and location in the 61 C. japonica plants analyzed.

 Genotype  Location  Seed oil content (%)  Seed oil content (g)
 jap-Brava 1  Areeiro  24.2  0.144
 jap-Brava 2  Areeiro  26.2  0.316
 71 - Furo-An  Areeiro  22.0  0.264
 91 - Yosemite  Areeiro  7.1  0.059
 108 - Shirobotan  Areeiro  13.3  0.145
 Pool of plants  Lourizán  28.3  0.213
 Pool of plants  Rubiáns  22.3  0.165
 Pool of plants  San Cibrán  22.6  0.214
 Average    20.8  0.190

 

Conclusion

      According to these results it is concluded that C. japonica seed oil production displays wide diversity and could be optimized by plant or genotype selection, based in seed traits, and that choice of an appropriate environment could bring further improvements in the seed oil content.

References

Huang, J., Ahrends, A., He, J., Gui, H., Xu, J., Mortimer, P. E. 2013. An evaluation of the factors influencing seed oil production in Camellia reticulata L. plants. Industrial Crops and Products 50: 797-802
Chang H.T., Bertholomew B. 1984. Camellias. Timber Press, Portland, USA.
Lin, C-Y., Fan, C-L. 2011. Fuel properties of biodiesel produced from Camellia oleifera Abel oil through supercritical-methanol transesterification. Fuel 90: 2240–2244.
Samartín, M. C., Pérez, A. 1988. La camelia, un regalo para Occidente. Everest. León, Spain.
Short, H. 2005. The truth of Lord Petre’s Camellias. The International Camellia Journal 37: 56-59.
Varela, C. P., Vazquez, J. P. M., Casal, O. A. 2003. First report of Phytophthora ramorum on Camellia japonica in Spain. Plant Disease 87: 1396-1396
Salinero C., Vela P. 2004. La Camelia en la colección de la Diputación de Pontevedra. Diputación de Pontevedra, Spain. 300 pp
Vela, P., Salinero, C., Sainz, M. J. 2013. Phenological growth stages of Camellia japonica. Annals of Applied Biology 162: 182–190.

 
 

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