Abstract
The present investigation was carried out during 2015–2017 to identify superior accessions of Garcinia lanceifolia Roxb., a highly medicinal fruit of Mizoram, North-east India. The ripe fruits of 25 selected accessions from six districts of Mizoram, north-east India were analyzed for fruit weight, fruit length, fruit diameter, fruit volume, pulp weight, peel weight, pulp: peel ratio, seed weight, seed length, seed diameter, number of seeds, TSS, acidity, ascorbic acid, reducing sugars and total sugars. The study reveals that there was significant variation among the accessions with respect to all these characters. Individual fruit weight ranged from 31.90 to 105.47 g; fruit volume 25.53–95.40 cm3; seed weight 12.98–46.98 g; peel weight 1.45–4.96 g; pulp weight ranged from 12.69 to 53.88 g. There was wide variation in chemical characters of the fruits also. TSS varied from 5.29 to 8.64%, titratable acidity varied from 3.27 to 5.72%, ascorbic acid 42.03–49.34 mg/100 g; total sugars 5.00–6.86%; reducing sugar ranged from 2.57 to 4.16%. From the results of the present investigation, MZU-HAMP-GC-1, MZU-HAMP-GC-2 and MZU-HAMP-GC-10 can be considered as elite G. lanceifolia Roxb. accessions for use in future breeding programmes.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
The genus Garcinia is a large genus of polygamous trees or shrubs belongs to the family Clusiaceae (Guttiferae) consisting of over 400 species of mostly small to medium sized trees. The genus is distributed in tropical Asia, Africa, and Polynesia more particularly in the southern part of Thailand and Peninsular Malaysia to Indonesia, and South East Asian region (Mabberley 2005). Among the various species of Garcinia in the world it is estimated that only 40 species produce edible fruits (Yapattanphum et al. 2002) of these some species are found to be domesticated as fruits of minor species. These include Garcinia atroviridis and Garcinia hombroniana in Malaysia; Garcinia indica in India; Garcinia multiflora in Vietnam and Garcinia pedunculata in Assam and Bangladesh. Species of the genus have various biological properties such as antioxidant (Muharni et al. 2009), cytotoxin (Wahyuni et al. 2004) and antimicrobial activities (Dachriyanus et al. 2004).
Garcinia is a source for a hydroxycitric acid (HCA) which is an anti-obesity compound present in the fruit rind and leaves of Garcinia (Cuong and Quang 2007). In India, about 35 species are found, many of which are endemic and economically important, with immense medicinal properties. The plants are found extensively in states such as Maharastra, Goa, coastal areas of Karnataka, Kerala, evergreen forest of Assam, Khasi and Jaintia hills of Meghalaya, West Bengal and Gujarat. Among the different species of India, 15 species are present in NE India and 8 species from Assam (Kar et al. 2008). G. pedunculata, Garcinia cowa, Garcinia lanceaefolia are the most important species of North-eastern India. Most species of Garcinia have several uses. Gambage is a gum resin which collected from Garcinia morella Dees distributed in India, Indo-China and southeast Asian region. A non-drying oil similar to Kokam butter, is extracted from the seeds of G. indica, G. morella and Garcinia cambogia for use in cooking and confectionary. Few species of Garcinia are used in traditional system of medicines. Some species have potential properties for treatment of HIV (Rukachaisirikul et al. 2003) and cancer (Nabandith et al. 2004). G. lancifolia is rich source of bioactive substances such as xanthones, biflavonoides, benzophenones with antimicrobial, cytotoxic and antioxidant acivities (Doley and Jha 2015; Chowdhury and Handique 2012).
Although Garcinia lanceifolia Roxb. is very important as a source of medicine in the socio-economic life of rural and tribal people of Mizoram, the information on extent of genetic variation among the accessions is very limited. Since the fruits are propagated only from seeds, there is tremendous variation among its population with respect to morphological and physico-chemical traits. In addition, due to lack of selection of any superior types among the population of the high valued species, the farmers have been planting seedlings of uncertain origin with low yield potential and quality. Till now, there is no concrete report on characterization of genetic diversity in the natural populations and no systematic studies have been undertaken to screen out superior genotypes of G. lanceifolia Roxb. in terms of physico-chemical properties of the fruits.
Although, newly developed molecular markers are valuable in gene based diversity studies, however the procedures used for the molecular markers analysis have disadvantage of high cost (Bouhadida et al. 2005). In contrast, morphological traits could feasibly be used for parental selection and along with molecular techniques are of highly appreciated procedures for description and germplasm classification of plants. Morphological criteria have been widely used as important markers in plant breeding programs (Kumar et al. 2015). Identification and description of the genetic variability available in the genotype are preliminary requirements for the exploitation of useful traits in plant breeding. The obtained data from the present investigation will be helpful to select the most promising genotype for use in breeding and to identify their desirable fruit and yield characteristics. The results will provide some guidance for screening of breeding resources for improving fruit quality and serve as a base for economically valuable phenotypes.
Use of available genetic resources is a major part of any crop improvement programme. The success of any improvement programme depends mostly on the identification and selection of superior parents for hybridization (Prakash et al. 2010). For improvement programme of any fruit crops, the rich gene pools incorporating extensive variability from basic ingredients are very important (Kumar et al. 2010). Therefore, exploitation of existing variability, identification of superior genotypes and their conservation are important in context of the present day scenario of rapid extinction of such useful unexploited fruit. Due to unawareness of the knowledge of biodiversity among local people, some germplasm is almost extinct and very little attention has been given for the characterization, evaluation and conservation of available accessions. In order to enrich the information and acquaint the breeders to interpret phenotypic values in terms of potential genetic gain, the present study was done to find out superior genotypes of G. lanceifolia Roxb.
Materials and methods
The present investigation was undertaken at six different districts of Mizoram, north-east India during 2015–2017 to assess the genetic diversity and identify the superior types of G. lanceifolia Roxb.
Mizoram, has an area of 21,081 km2 and lies between 21°56′N and 24°31′N latitude and 92°16′E and 93°26′E longitude. The state has international borders with Bangladesh in the west and Myanmar in the east and south. On the northern side it borders with three states of India viz. Tripura in north west, Assam in north and Manipur in the north east. Being sandwiched between Bangladesh and Myanmar, its location is geographically and politically significant (Fig. 1). The hilly state is covered with tropical and subtropical forest cover. It is one of the hot spots of biodiversity.
Garcinia lanceifolia Roxb. trees are found scattered throughout the states from homestead garden to forest areas. The collection of fruits from six districts i.e. Aizawl, Serchhip, Lunglei, Kolasib, Mamit and Champhai comprising of 25 different accessions was conducted during the fruiting season of 2015–2017. Details of the accessions and their sources are given in Table 1. The collected fruits were immediately brought to the Post-harvest Laboratory, dept. of HAMP, Mizoram University for analysis of Physio-chemical characters.
For measuring the physical parameters of the fruits, 20 randomly selected fruits were taken from each replication. Quality parameters like juice, TSS, acidity, ascorbic acid, reducing, non-reducing and total sugars were estimated following standard procedures. The standard method (AOAC 1995) was followed to determine the qualitative parameters of fruit. The data obtained from different observations during field experimentation and laboratory analysis were subjected to Fisher’s method of analysis of variance (ANOVA) by following completely randomized design. Significance and non-significance of the variance due to different treatments were determined by calculating the respective ‘F’ value and comparing with the appropriate value of ‘F’ at 5% probability level (Panse and Sukhatme 1985). By comparing different treatments among themselves critical difference were calculated at 5% probability level.
Results and discussion
Among all the accessions, the highest fruit weight was recorded in MZU-HAMP-GC-10 (105.47 g) which was followed by MZU-HAMP-GC-1 (101.96 g), and MZU-HAMP-GC-2 (99.34 g) (Table 2). Similarly, the maximum fruit length was recorded in MZU-HAMP-GC-1 (57.80 mm), which was significantly higher than all other accessions except MZU-HAMP-GC-2 (53.41 mm), and MZU-HAMP-GC-10 (53.01 mm), with which it was statistically at par. This variation in fruit length might be due to different genetic make-up of the genotypes (Hazarika et al. 2013a).
The maximum fruit diameter (67.17 mm), and fruit volume (95.66 cm3) was recorded in MZU-HAMP-GC-10. There was no significant difference among the accessions with respect to specific gravity (Table 2). However, MZU-HAMP-GC-3 (1.24) and MZU-HAMP-GC-18 and MZU-HAMP-GC-11 (1.03), recorded the highest and lowest value of specific gravity. The highest number of locules was observed in MZU-HAMP-GC-10 (8.24), followed by MZU-HAMP-GC-2 (7.97), MZU-HAMP-GC-1 (7.84), and MZU-HAMP-GC-21 (7.53). The variation in locules number might be due to different genetical constitution of the individual genotypes. Our study is in close conformity with the findings of Hazarika et al. (2013b), who also obtained significant variation in number of segments among different accessions.
Peel weight and pulp weight of the accessions ranged between 1.45–4.96 g and 12.69–53.88 g respectively. MZU-HAMP-GC-2 recorded the highest peel weight (4.96 g), which was significantly higher than all other accessions except MZU-HAMP-GC-1 (4.91 g), and MZU-HAMP-GC-10 (4.61 g), whereas, MZU-HAMP-GC-10 (53.88 g), recorded the highest pulp weight, followed by MZU-HAMP-GC-1 (51.54 g), and MZU-HAMP-GC-2 (50.64 g). Our finding is in agreement with the findings of Hazarika et al. (2017).
The analysis of variance presented in Table 2 revealed a correlation among fruit weight and pulp weight. The genotypes produced higher fruit weight may be due to more pulp weight. This clearly indicated that, during selection of any genotype based on fruit, the breeder should give emphasis on fruit pulp content rather than fruit weight alone. Our study is in close conformity with the findings of Hazarika et al. (2013b), who also obtained significant variation in pulp weight among a number of accessions.
In the present study, there was no significant difference among the accessions with respect to pulp peel ratio (Table 2). However, MZU-HAMP-GC-10 (11.79) and MZU-HAMP-GC-3 (6.47), recorded the highest and lowest value of pulp peel ratio.
It is evident from the data presented in Table 2 that the accessions varied significantly with respect to seed characters. MZU-HAMP-GC-1 recorded the highest number of seeds (6.83), followed by MZU-HAMP-GC-10 (6.41), MZU-HAMP-GC-2 (6.23), MZU-HAMP-GC-12 (6.06), MZU-HAMP-GC-13 (6.03) and MZU-HAMP-GC-9 (5.92) (Table 2). Likewise, the maximum seed weight (46.98 g) and seed length (13.19 mm) was observed in MZU-HAMP-GC-1. Similarly, MZU-HAMP-GC-13 recorded the highest seed diameter (17.95). The variation in seed characteristics among the different accessions may be due to different genetical constitution of the individual genotypes. The variation in seed characters might be due to genetical constituents of the accessions (Hazarika et al. 2016).
The accessions varied significantly with respect to quality parameters of the fruits. Among all the accessions, the highest moisture percent was recorded in MZU-HAMP-GC-10 (94.77%), which was followed by MZU-HAMP-GC-1 (94.68%) and MZU-HAMP-GC-23 (93.97%) (Table 3). The highest value of TSS was recorded in MZU-HAMP-GC-10 (8.64%). The variation in TSS may be due to different genetical constitution of the individual genotypes. Fruits growing in an arid region with limited water tended to more accumulation of dry matter and lower moisture content which may result in higher TSS in fruits (Meghwal and Azam 2004). The breeders during selection of superior genotypes should emphasize total soluble solids content of the fruits. Korikanthimath and Desai (2006) and Patil et al. (2005) reported variation in TSS among a number of Garcinia species.
Ascorbic acid is also one of the most important criteria, which also determine the quality of fruits. In our study, the highest value of ascorbic acid was recorded in MZU-HAMP-GC-1 (49.34 mg/100 g) followed by MZU-HAMP-GC-10 (48.43 mg/100 g), and MZU-HAMP-GC-2 (47.45 mg/100 g). Our study is in close conformity with the findings of Hazarika et al. (2013b), who also obtained significant variation in ascorbic acid content of the fruits. Similarly, MZU-HAMP-GC-2 (3.27%), recorded the lowest titratable acidity which was significantly lower than all other accessions except MZU-HAMP-GC-1 (3.42%), and MZU-HAMP-GC-10 (3.45%), with which it was statistically at par. The highest acidity was recorded in MZU-HAMP-GC-7 (5.72%). This is a fact in many fruits that, when TSS is increasing acidity is decreased. This may be major factor for minimum acid content in MZU-HAMP-GC-2, MZU-HAMP-GC-1 and MZU-HAMP-GC-10. The variation among genotypes for acidity might be due to genetic make of plant (Prakash et al. 2010) which has also proved in our study.
There was significant variation among the accessions with respect to sugar content also. The highest value of total sugars (6.86%), and reducing sugars (4.16%) was recorded in MZU-HAMP-GC-10 which was significantly higher than most of the accessions. MZU-HAMP-GC-22 (4.14%) recorded the highest value of non-reducing sugars followed by MZU-HAMP-GC-25 (3.67%), MZU-HAMP-GC-16 (3.40%), MZU-HAMP-GC-6 (3.24%), and MZU-HAMP-GC-2 (3.17%). The variation in sugar content among the accessions may be due to different genetical constitution of the individual genotypes.
The variation among the different accessions in sugar: acid ratio was also found significant (Table 3). Among all the accessions, MZU-HAMP-GC-2 recorded highest value of sugar: acid ratio (2.09) but it was found statistically at par with MZU-HAMP-GC-10 (2.00), and MZU-HAMP-GC-1 (1.93). The significantly lowest sugar: acid ratio was recorded in MZU-HAMP-GC-12 (1.02). Variation in sugar:acid ratio among a number of accessions was also reported by Singh and Singh (2003). Similarly, the highest TSS: acid ratio was recorded in MZU-HAMP-GC-2 (2.59), followed by MZU-HAMP-GC-10 (2.52), and MZU-HAMP-GC-1 (2.50).
Preference of consumers always depends on physical parameters of fruits like fruit weight, fruit diameter, pulp content and pulp: peel ratio of any fruit. In G. lanceifolia Roxb. more fruit weight, bigger size, more pulp content and pulp: peel ratio, greater is the acceptability by the consumer. Likewise, among the biochemical constituents of the fruits, consumers always prefer the fruits with high juice content, ascorbic acid, TSS, low acidity and high sugar: acid ratio. Similarly, for development of a new cultivar, breeders also choose accessions with these desirable qualities. From the summary of the present investigation, it has been observed that, among all the accessions of G. lanceifolia Roxb. collected from different locations of Mizoram, MZU-HAMP-GC-1, MZU-HAMP-GC-2 and MZU-HAMP-GC-10 having all the desirable physical and chemical parameters for the farmer, consumer as well as breeders. Therefore, from the present investigation, it can be concluded that MZU-HAMP-GC-1, MZU-HAMP-GC-2 and MZU-HAMP-GC-10 can be considered as elite G. lanceifolia Roxb. accession for use in various purposes from Mizoram, north-east India.
References
AOAC (1995) Official methods of analysis, 16th edn. Association of Official Analytical Chemists, Washington
Bouhadida M, Casas AM, Moreno MA, Gogorcena Y (2005) Genetic diversity of prunus rootstock using microsatellite markers. Acta Hortic 771:25–31
Chowdhury T, Handique PJ (2012) Evaluation of antibacterial activity and phytochemical activity of Garcinia lancifolia Roxb. Int J Pharma Sci Res 3:1663–1667
Cuong DH, Quang DV (2007) Estimating hydroxycitric acid in leaves, rinds, fruits of Garcinia oblongifoia champ. ex benth by HPLC. J Sci Technol Danang Univ 3:137
Dachriyanus D, Izati M, Fahmi R (2004) Antimicrobial compounds from the bark of Garcinia parvifolia Mig. Jurnal Matematika & Pengetahuan Alam 13(1):20–24
Doley P, Jha DK (2015) Antimicrobial activity of bacterial endophytes from medicinal endemic plant Garcinia lancifolia Roxb. Ann Plant Sci 4:1243–1247
Hazarika TK, Lalawmpuii B, Nautiyal BP (2013a) Studies on variability in physio-chemical characters of hatkora (Citrus macroptera Mont.) collections of Mizoram. Indian J Hortic 70:480–484
Hazarika TK, Merilyn L, Nautiyal BP (2013b) Genetic variability in physico-chemical characteristics of some pummelo collections from Mizoram. Indian J Hortic 70:431–434
Hazarika TK, Lalthlamuani, Lalchhanmawia J, Lalrinfeli, Nautiyal BP (2016) Variability in physico-chemical characteristics and selection of superior types among local pummelo (Citrus grandis (L.) Osbeck) germplasms from Mizoram, North East India. Curr Sci 111:1355–1361
Hazarika TK, Lalchhanmawia J, Lalrinfeli L, Shukla AC, Nautiyal BP (2017) Assessment of genetic variability in the endangered Citrus macroptera Mont. (“hatkora”) from Mizoram, north-east India. Genet Resour Crop Evol 64:321–330
Kar A, Borkakoti S, Borthakur SK (2008) Extended distribution of the genus Garcinia L. in Sonitpur district, Assam, India. Pleione 2:165–170
Korikanthimath VS, Desai AR (2006). Status of Kokum (Garcinia indica Choicy) in Goa. Compadium on Kokum (Garcinia indica), 2nd National Seminar on Kokum (Garcinia indica Choicy) held at Goa University during 4–5 Mar, 2005, pp 17–27
Kumar PS, Devi P, Choudhary VK, Kanwat M (2010) Evaluation of different mandarin, sweet orange rootstock species and cultivars under mild hill conditions of Arunachal Pradesh. Indian J Hortic 67:433–440
Kumar D, Lal S, Ahmed N (2015) Morphological and pomological diversity among Apricot (Prunus armeniaca) genotypes grown in India. Indian J Agric Sci 85(1):349–355
Mabberley DJ (2005) The plant book A, portable dictionary of the vascular plants, 2nd edn. Cambridge University Press, Cambridge, p 293
Meghwal PR, Azam MM (2004) Performance of some aonla cultivars in arid region of Rajasthan. Indian J Hortic 61:87–88
Muharni M, Supriyatna S, Bahti HH, Dachriyanus D (2009) Phenolic compound from the stem bark of manggis hutan (Garcinia bancana Miq.) and their antioxidant activity. Indones J Chem 9(2):321–327
Nabandith V, Suzui M, Morioka T, Kaneshiro T, Kinjo T, Matsumoto K, Akao Y, Iinuma M, Yoshimi N (2004) Inhibitory effects of crude alpha-mangostin, a xanthone derivative, on two different categories of colon preneoplastic lesions induced by 1, 2-dimethylhydrazine in the rat. Asian Pac J Cancer Prev 5(4):433–438
Panse VG, Sukhatme PV (1985) Statistical methods for agricultural workers. ICAR, New Delhi
Patil BP, Gawankar MS, Sawant DS, Pujari KH, Jambhale ND (2005) Cultivation of Konkan Amruta and Search for elite varieties. In: Preview of 2nd national seminar on kokum, 4–5th Mar. Goa University, Goa, pp 29–34
Prakash J, Maurya AN, Singh SP (2010) Studies on variability in fruit characters of jamun. Indian J Hortic 67:63–66
Rukachaisirikul V, Pailee P, Hiranrat A, Tuchinda P, Yoosook C, Kasisit J, Taylor WC, Reutrakul V (2003) Anti HIV-1 protostane triterpenes and digeranyl benzophenone from trunk, bark and stems of Garcinia speciosa. Planta Med 69:1141–1146
Singh IP, Singh S (2003) Exploration, collection and mapping of Citrus genetic diversity in India. Technical bulletin no. 7, NRC for Citrus, Nagpur, pp 230
Wahyuni FS, Lindsay TB, Dachriyanus DR, Jubahar J, Lajis NH, Sargent MV (2004) A new ring-reduced tetraprenyltoluquinone and a prenylated xanthone from Garcinia cowa. Aust J Chem 57:223–226
Yapattanphum C, Subhadrabandhu S, Sugiura A, Yonemori K, Utsunomiya N (2002) Utilization of some Garcinia species in Thailand. Acta Hortic 575(2):563–570
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that there is no conflict of interest in whatsoever.
Rights and permissions
About this article
Cite this article
Hazarika, T.K., Lalnunsangi, C. Exploring genetic diversity of Garcinia lanceifolia Roxb. (Clusiaceae), a highly medicinal and endangered fruit of north-east India. Genet Resour Crop Evol 66, 61–69 (2019). https://doi.org/10.1007/s10722-018-0695-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10722-018-0695-5