1 - 2 cm long shoot tips and fruits (for zygotic embryos) were collected of both cultivars (Purbi and Bedana) of litchi growing at Horticulture Division, Bihar Agricultural College, Sabour, Bhagalpur, Bihar, INDIA. Both shoot tips and fruits (for zygotic embryos) were taken with a 15 days interval from March to June because both initiated in the same time and in this duration phenolic concentrations are low and browning of explants during excision could be controlled under in-vitro condition. These immature fruits and shoot tips were washed in running tap water for the removal of dust particles. Followed by these immature litchi fruits and shoot tips were dipped in to tap water mixed with 2 - 4 drops of Tween 20 and swirled so that foam were formed and remained there for 6 - 7 minutes after that these fruits and shoot tips were taken out, washed in running tap water and again dipped them in 1% bavistin for removal of fungal surface contamination. Followed by these immature Litchi fruits and shoot tips were dipped for 10 min in sodium hypochlorite (1% activated chlorine) containing a few drops of Tween 20, rinsed three times in sterile-distilled water and again dipped in 0.1% HgCl₂ for 5 - 7 minutes under sterile condition and remained there for 5 - 6 minutes. Followed by HgCl₂ was decanted, rinsed thrice in autoclaved glass distilled water and then surface sterilized fruits wall were removed with the scalpel blade and both zygotic embryos and shoot tips were taken out in sterile condition. Now both explants (zygotic embryos and shoot tips) were ready for experiments.

Formulation of media used in the experiments

Different media which are used in these experiments have been formulated in (Table 1).

Shoot tip and zygotic embryo culture

50 shoot tips were excised under aseptic conditions and inoculated on medium MS1 (see Table 1). Followed by inoculation, the cultures were incubated at 25˚C ± 2˚C under cool-white fluorescent illumination with 16 h day-length. After three weeks, the percentages of browning of explants were determined. The dead explants because of the browning were discarded, while surviving explants were sub-cultured to the fresh media.

Determination of total phenolic content

For total phenolic extraction, shoot tips and zygotic embryos were homogenized with 50% ethanol in water and left for 2 h in the dark. After filtration the concentration of

total phenolics in the shoot tips and zygotic embryos were determined by the Folin- Ciocalteu colorimetric method ( Singleton & Rossi, 1965 ). Estimations were carried out in triplicate and calculated from a calibration curve obtained with gallic acid. Total phenolic contents were expressed as gallic acid equivalents (mg GAE/g).

HPLC separation of phenolic compounds

Phenolic compounds were extracted from shoot tips and zygotic embryos as described by KarKacier (1998) . Briefly, 2.5 grams of shoot tips were mixed with 5 ml of HPLC-water, presence of ascorbic acid to prevent the oxidation. The mixture was homogenized by using ultratorax at 24,000 rpm and centrifuged at 6000 rpm for 30 min at ambient temperature. Then, 2.5 ml of mixture was diluted with 2.5 ml of HPLC water. After centrifuging at 6000 rpm, the final mixture was filtered through 0.45 μm membrane filters before 20 μl injections. High Pressure Liquid Chromatography (HPLC) analysis of phenolics was performed by HPLC on a Varian Model 9010 equipped with a UV-visible (Varian 9010 Model) detector and an auto sampler ( Marathon ). Gradient elution was performed with 5% formic acid (Merk, eluent A) and methanol (Merk, eluent B), and gradient programme followed as 0 - 8 min 70% A - 30% B, 8 - 8.5 min 65% A - 35% B, 8.5 - 20 min 60% A - 40% B, 20 - 30 min 54% A - 46 B, 30 - 30.5 min 40% A - 60% B, 30.5 - 34.5 min 15% A - 85% B and 34.5 - 35 min 70% A - 30% B. The UV detection was performed at 280 nm. The elution was conducted at room temperature using a Supelco C₁₈ column (15 × 4.6 I.D.), and at a flow rate of 1 ml/min.

Initial identity assignment of phenolic was based on comparison retention data obtained with UV detector for standard compounds and sample compounds. Quantization was achieved by using peak areas from external calibration with standard [gallic acid, catechol, quercetin, rutin, o-coumeric acid (sigma), chlorogenic acid and +(−) catechin (FluKa)] solutions. All determinations were done three times by using three different samples and data are expressed μg/g fresh weight.

MS2 medium for callus (friable) development in semi-solid culture

Shoot tips and zygotic embryos were inoculated on MS2 media (see Table 1) separately in petridish, placed them in dark condition, incubated at 25˚C ± 2˚C for 4 months and were sub-cultured in every 2 weeks interval.

MS3 medium for suspension culture

MS3 medium (see Table 1) supplemented with different concentration of ascorbic acid i.e. 1, 2, 3, 5, 10 mgl⁻¹ were mixed and made the volume 1 litre, adjust the pH 5.6 - 5.8, dispensed into 50 ml in each 250 ml volume Erlenmeyer conical flask and autoclaved. In each flask friable callus was put, mixed and placed on 120 rpm agitated orbital shaker incubated at 25˚C ± 2˚C for 8 weeks and were sub-cultured in every 2 weeks.

MS4 medium for liquid culture

Immature or matured litchi seeds (for zygotic embryos) were cultured in culture tubes having MS4 medium (see Table 1) of 20 ml in each culture tubes with filter bridge and placed them in standard cultural condition (light intensity 60 μE m⁻²∙s⁻¹, period 16 h l/8h d and incubated at 25˚C ± 2˚C) for 16 weeks and were sub-cultured in every 2 weeks interval.

Different concentrations of Activated charcoal (1 gl⁻¹, 2 gl⁻¹, 2.5 gl⁻¹, 3 gl⁻¹, 4.5 gl⁻¹ and 5 gl⁻¹) were prepared and this Activated charcoal were separately added before autoclaving of MS2, after that autoclaved MS2 medium were poured in sterilized Petri plates and left it for polymerization. After solidification of medium in each Petri plates 6 shoot tips and zygotic embryos were inoculated separately in each separate petriplates and petri plates were sealed with parafilm, kept them in culture room in dark condition at 25˚C ± 2˚C temperature up to four months, sub-cultured in every 2 weeks interval and observe their effects.

Different concentrations (25 mM, 50 mM, 75 mM, 100 mM, 125 mM and 150 mM) of L-cysteine HCl were prepared separately and were sterilized through micro filter unit. Followed by shoot tips and zygotic embryos were presoaked in this solution for 45 minutes, inoculated on MS2 medium. L-cysteine HCl is used only in presoaking of zygotic embryos to minimize browning during excision but it is not supplemented in the medium.

1) At low concentration

Different concentrations (0.025 gl⁻¹, 0.050 gl⁻¹, 0.075 gl⁻¹, 100 gl⁻¹ and 150 gl⁻¹) of Ascorbic acid were prepared, sterilized as above and were mixed separately into autoclaved cooled MS2 medium. After that shoot tips and zygotic embryos were inoculated separately in plates and were kept in culture room in dark condition.

2) At high concentration

All conditions and media were same as mentioned above but only Ascorbic acid was prepared of (1 gl⁻¹, 2 gl⁻¹, 2.5 gl⁻¹, 3 gl⁻¹, 5 gl⁻¹ and 10 gl⁻¹) different concentrations.

3) Presoaked zygotic embryo in ascorbic acid

Shoot tips and Zygotic embryos were presoaked in 3 gl⁻¹ Ascorbic acid solution for 2 hour and were inoculated on MS2 media with BAP 200 mgl⁻¹ and different (1 gl⁻¹, 2 gl⁻¹, 2.5 gl⁻¹, 3 gl⁻¹, 5 gl⁻¹ and 10 gl⁻¹) concentrations of ascorbic acid. Followed by all plates were kept into culture room in dark condition incubated at 25˚C ± 2˚C.

Different concentrations (0.025 gl⁻¹, 0.050 gl⁻¹, 0.075 gl⁻¹, 0.100 gl⁻¹ and 0.150 gl⁻¹) of Ascorbic acid were prepared, sterilized through filter unit and were mixed separately into autoclaved cooled MS2 with 2.5 gl⁻¹ Activated Charcoal medium. Followed by the inoculation of shoot tips and zygotic embryos, all plates were kept in culture room in dark condition incubated at 25˚C ± 2˚C.

1) Without presoaked shoot tips and zygotic embryos in ascorbic acid

Different concentrations (1 gl⁻¹, 2 mgl⁻¹, 3 gl⁻¹, 4 gl⁻¹ and 5 gl⁻¹) of Citric acid were prepared, sterilized through filter unit and were mixed separately into autoclaved cooled MS2 medium and after the inoculation of shoot tips and zygotic embryos all plates were kept in culture room in dark condition at 25˚C ± 2˚C.

2) Presoaked zygotic embryo in ascorbic acid

Shoot tips and Zygotic embryos were presoaked in 3 gl⁻¹ Ascorbic acid solution for 2 hour and they were inoculated on MS2 media with different concentrations (1 gl⁻¹, 2 gl⁻¹, 3 gl⁻¹, 4 gl⁻¹ and 5 gl⁻¹) of Citric acid and all plates were kept in culture room in dark condition and incubated at 25˚C ± 2˚C.

Different concentrations (25 mM, 50 mM, 75 mM, 100 mM, 125 mM and 150 mM) of AgNO₃ were prepared separately and were sterilized through micro filter unit. After that both shoot tips and zygotic embryos were presoaked in this solution for 45 minutes and then were inoculated on MS2 medium supplemented with different concentration of AgNO₃ and kept on dark condition incubated at 25˚C ± 2˚C.

Different concentrations of Ascorbic acid (0.200 gl⁻¹, 0.500 gl⁻¹, 1 gl⁻¹, 1.5 gl⁻¹ and 2 gl⁻¹) and the same concentration of Citric were prepared, mixed together separately and made the citric and ascorbic acid solution (combined). Both the explants (shoot tips and zygotic embryos) were presoaked in 0.225 gl⁻¹ citric with ascorbic acid solution and were inoculated on MS2 medium supplemented with different concentration of ascorbic acid and citric acids combined and kept on dark condition incubated at 25˚C ± 2˚C.

Three replicas were made for all experiments.

To see the effect of filter bridge with ascorbic acid on control of browning, germinability and multiple shoot induction from zygotic embryos in liquid culture, immature or mature seeds were inoculated on MS4 medium supplemented with BAP 20 mgl⁻¹, ascorbic acid 5 mgl⁻¹ with or without filter bridge and placed them in standard cultural conditions for 4 - 6 weeks. Since zygotic embryos immature or matured during excision from seeds secretes comparatively a large amount of phenolics so that instead of zygotic embryos, immature or matured seeds were cultured on filter bridge in liquid medium which secretes comparatively less amount of phenolics.

Data for explants browning were subjected to angular transformation for normalizing the frequency distribution, prior to statistical analysis. In each experiment 6 explants for control of browning were taken in each petridish and three petridishes for each treatment and 100% of control of browning of explants’ response was observed in combined effect of ascorbic and citric acids. The percentage response of calli production from explants was different in different antioxidants concentrations i.e. from 1 to 80 in semi-solid culture of six explants cultured and maximum 3 × 10⁶ number of cells/ml in suspension culture. The statistical significance on phenolic composition of explants (shoot tips and zygotic embryos) was calculated by one-way ANOVA followed by Tukey’s multiple comparison tests. All data analyses were performed using the Graph Pad software (Graph Pad in Stat. Software Inc., San Diego, CA 92130, USA).

Some of the explants cultured in vitro remained viable and grew during the establishment stage of the in vitro culture, while some of them turned dark brown. A major browning phenomenon was observed after about 12 - 14 days of inoculation. The data recorded after three weeks for the explants browning and the statistical separation of the means are given in Table 2(a) & Table 2(b). The percentages of explants’ browning changed significantly according to cultivars and the months of the explants collection (p ≤ 0.05). In both cultivars, the lowest percentages of explants browning were detected in the shoot tips and zygotic embryos collected in March and explants browning gradually increased during the season, with high values in Bedana. Both zygotic embryos (as immature litchi fruits) and shoot tips were collected after four weeks of anthesis (i.e. opening of flower, pollination and fertilization of egg and polar nuclei with male gametes accomplished in ovule inside ovary) in the same month i.e. March (Reproductive stage), because both inflorescences, which later developed zygotic embryos after anthesis inside immature fruit, and shoot tips, sprouted in same time during spring season. Both were used as explants in vitro culture for callus development and somatic embryogenesis from zygotic embryos and multiple shoot induction and plant regeneration from shoot tips for mass scale propagation. It has been observed that in both explants the concentration of phenolics is comparatively low in March and consequently browning which is caused by the oxidation of phenolics by Polyphenoloxidase and formed melanin pigment (brown in color), necrosis and death of explants was under control during in vitro culture. Both explants responded well in callus proliferation from zygotic embryos and multiple shoot induction from shoot tips during march but as months forward i.e. from April to June browning was comparatively higher due to increase in phenolic compounds concentration, in June it is out of control, explants showed heavy browning, necrosis and death of explants and consequently no or a few callus developed during in-vitro culture.

Mean value of three individual experiments showing significant *, more significant ** and most significant *** respectively in both Table 2(a) & Table 2(b), ±Standard Error. Purbi ***P < 0.001, ** P < 0.01, *P < 0.05, Bedana ***P < 0.001, **P < 0.01, *P < 0.05.

Total phenolic contents of shoot tips and zygotic embryos in the various months are presented in Table 2(a) & Table 2(b). Genotype and months of explants collection had significant effects on the total phenolic contents in shoot tips and zygotic embryos (p ≤ 0.05).

Total phenolic content in the Purbi shoot tips and zygotic embryos exhibited a low initial value in March, and then increased gradually, reaching a maximum level in June. Although Purbi showed a similar pattern for total phenolic content with Bedana, this litchi cultivar exhibited higher total phenolic contents than Bedana in all months.

No response of explants in the browning control was observed in different concentrations of activated charcoal (1, 1.5, 2.0, 2.5, 3.0 and 3.5 gl⁻¹), pre-soaking of explants with or without activated charcoal in L-cysteine HCl (25, 30, 75, 100, 125 and 150 mM), low concentration of ascorbic acid (0.025, 0.050, 0.075, 0.100, 0.150 gl⁻¹) and AgNO₃ (25, 50, 75, 100 and 125 mM).

1) At high concentration

During soaking of explants(shoot tips/zygotic embryos) with high concentration of ascorbic acid all were fresh after inoculating them on MS2 medium supplemented with ascorbic acid, all explants were fresh and better result was observed at 3 gl⁻¹ and within 6 - 7 weeks callus formation was started (see Table 3) (Figure 1, Figure 2 & Figure 4).

2) Ascorbic acid with activated charcoal

Explants were showing fresh next two weeks after the culturing on MS2 medium supplemented with both ascorbic acid and charcoal, but after two weeks it turned into pale and gradually browning was appeared. Best result was observed at 2.5 gl⁻¹ and 3.5 gl⁻¹ and formation of callus taken place (see Table 4).

After culturing of explants (shoot tips/zygotic embryos) on MS2 medium supplemented with different concentration of citric acid, all were fresh but after three weeks in turned into pale, but presoaking of explants on citric acid and again culture on MS2 medium with same condition all were fresh and formation of somatic embryos were taken place (see Table 5).

All explants (shoot tips/zygotic embryos) when cultured on MS2 medium supplemented with combined different concentrations of ascorbic acid and citric acid, were fresh and formation of somatic embryos started and best result was observed at 1 gl⁻¹ - 1.5 gl⁻¹ concentration of ascorbic with citric acid (see Table 6).

It was observed that following 4 - 6 weeks immature or matured seeds (for zygotic embryos) cultured on MS4 medium (liquid) on filter bridge they induces about 6 - 9 multiple shoots on cotyledonary node in presence of less concentration of ascorbic acid 5

mgl⁻¹ browning was controlled may be due to settling down of phenolics on filter bridge and also in liquid medium. Those seeds which were cultured in the medium without filter bridge shoot buds were not induced on cotyledonary node. It was also observed that following 4 - 6 weeks Filter Bridge were turned brown may be due to binding of phenolics on filter bridge ( Das et al., 1999a, b ) (Figure 3).

Cells grown in suspension culture both from shoot tips and zygotic embryos separately in MS 3 liquid medium were fresh at 2 mgl⁻¹ concentration of ascorbic acid. The cells were observed growing very fast and cells were fresh. The secretion of phenolics in the medium was also controlled but both in lower and higher concentration of ascorbic acid a small number of cells were grown and degree of control of browning was less effective. In control where ascorbic acid was not added in the medium both cells and medium were turned brown (see Table 7) (Figure 4).

Role of antioxidants on browning control

Activated charcoal has large number of pore & active binding sites for polyphenols and for other compounds in most of the cases it was observed that it was able to control browning as well as inhibitory compounds but in the case of litchi activated charcoal alone was not found able to control the browning and it could be due to binding with some nutrients also.

Ascorbic acid is a potent antioxidant it has been frequently used for browning control ( Toth et al., 1993 ), it reduced the polyphenoloxidase activity in the case of litchi can check the browning when explants presoaked into ascorbic acid solution just after the excision of zygotic embryo and culture it at high concentration on ascorbic acid with or without activated charcoal because embryo secretes large amount of phenolic compounds just after incision of explants.

The combination of ascorbic with citric acid acts as a powerful antioxidant it may inhibit the polyphenoloxidase activity and also serve as a vitamin so that it is able to check the browning and initiate proliferation of cells and somatic embryo arises from explants.

It was observed that when explants of Pistachio species was 15 min. soaked in L- cysteine HCl at 100 mM before the culturing it eliminates the browning ( Gannoun et al., 1995 , Tabiyeh et al., 2006 ) as well as increases the shoot bud formation but when this treatment applied for Litchi initially all explants were fresh but after the one week browning appeared gradually.

AgNO₃ is an ethylene inhibitor and inducer for adventitious shoot bud formation ( Rouston et al., 2008 ) as well as control the browning of Pistachio. But in case of Litchi it was observed that it is not effective to check the browning.

Finally it was observed that both excision and incision of zygotic embryos and shoot tips under axenic condition and use of ascorbic acid 2.5 gl⁻¹ with activated charcoal 2 gl⁻¹, ascorbic acid 3 gl⁻¹ after pre soaking in 3 gl⁻¹ ascorbic acid solution and a combination of ascorbic acid 1.5 gl⁻¹ and citric acid 1.5 gl⁻¹ pre soaking in 3 gl⁻¹ ascorbic acid solution and frequent sub-culturing in semi-solid culture can eliminate the browning and reduced the polyphenoloxidase activity of Litchi. But in contrary, suspension culture browning could be controlled at very low concentration of ascorbic acid than the semi-solid culture could be due to cells are in direct contact of medium having ascorbic acid (antioxidants) and absorbs from whole cells surface but if concentration will increase up to 10 mgl⁻¹ then browning couldn’t be controlled by ascorbic acid could be due to attainment of inhibitory action of ascorbic acid in suspension culture.

The amounts and variations of phenolic compounds in the shoot tips and zygotic embryos collected in the different months are presented in Table 2(a) & Table 2(b). The genotype as well as the month of explants collection seemed to the major factors influencing the relative concentration of the various phenolic compounds in the shoot tips and zygotic embryos. In both cultivars, the various phenolic compounds quantified in this study showed significantly differences in shoot tips and zygotic embryos collected in different months (p ≤ 0.05).

Gallic acid and +(−) catechin were the most abundant phenolic compounds in the shoot tips and zygotic embryos in both cultivars, with higher concentration in Purbi. In both cultivars, the lowest concentrations for gallic acid were found in the shoot tips and zygotic embryos collected in March. But gallic acid concentration increased at different rates up to June. Concentrations of +(−) catechin in Purbi shoot tips and zygotic embryos significantly increased from March to May but there was no any significant difference for +(−) catechin between May to June. In Bedana +(−) catechin also showed a gradual increase during the season and the highest value was detected in the shoot tips and zygotic embryos collected in June. The amounts of the second most abundant phenolic compounds in shoot tips and zygotic embryos were catechol and chlorogenic acid. In Purbi, catechol concentration was relatively low in the shoot tips and zygotic embryos collected in March. But it subsequently exhibited a strong increase in the explants collected in April. After that this increase, but more slightly, continued up to June. Bedana also exhibited almost similar pattern with Purbi for +(−) catechin. Concentrations of chlorogenic acid in the shoot tips and zygotic embryos were higher in Purbi than Bedana, in all months. While concentration of chlorogenic acid in Purbi did not significantly vary in the shoot tips and zygotic embryos collected in March, April and June, it showed a significantly increase in June. Although a lower chlorogenic acid concentration in Bedana was found in the shoot tips and zygotic embryos collected in June compared the shoot tips and zygotic embryos collected in the previous months, the values did not differ significantly. The amounts of rutin in Purbi remained almost stable from March to May, but it showed a strong increase in the shoot tips and zygotic embryos collected in June. On the other hand in Bedana concentration of rutin gradually increased during summer and reached to maximum value in June. Concentration of o-coumaric acid in shoot tips and zygotic embryos of Bedana gradually increased during summer as it showed a sharp decrease from March to June in Purbi. The highest concentration of quercetin in Purbi was found in the shoot tips and zygotic embryos collected in April, and there was no any significant difference among the other month. Quercetin content of Bedana had a different pattern to that of Purbi. Although it differed slightly from March to June, these differences were not significant.

Correlation coefficients between the explants browning and the phenolic compounds were given in Table 8. The most remarkable positive correlation was found between explants browning and the total phenolic content. Gallic acid, +(−) catechin, catechol and chlorogenic acid in the explants exhibited a significantly strong positive correlation with the explants browning. But explants browning showed relatively weak positive relationship with rutin. Neither the concentration of o-coumeric acid, nor that of quercetin showed a significant relationship with the explants browning.

Browning and subsequent death of explants is a common problem in cultures of woody plants and has generally been attributed to the oxidation of phenolic compounds in explants tissues ( Hu & Wang, 1983 ). Browning is of considerable importance, because it invariably leads to the death of the explants.

In this study, it was determined that the browning percentages of explants varied significantly depending on the cultivars. Shoot tips and zygotic embryos of Purbi exhibited higher explants browning than those of Bedana when their percentages were compared in the same months. It has been observed that the explants browning is highly genotype dependent, as previously reported by Tangolar et al. (1999) , Thomas & Ravindra (1997) and Yu & Meredith (1986) .

Time of explants collection is in general a critical factor in explants browning ( Dalal et al., 1993 ; Dhar & Upreti, 1999 ; Tangolar et al., 1999 ; Thomas & Ravindra, 1997 ). In both cultivars, the lowest explants browning percentages were found in the shoot tips and zygotic embryos collected in March> Shoot tips and zygotic embryos collected in the other months showed more browning, turned brown sooner and showed no growth response similar reported by Baydar, 2006 in grapevine. But Fanizza et al. (1984) in grapevine, Roussos & Pontikis (2001a, b) in olive found that season of explants collection did not influence the explants browning.

*P ≤ 0.05, ***P ≤ 0.0001, ns: not significant, n = 84.

Time of explants collection influences not only the percentage of explants browning but also the contents of total phenolics ( Dalal et al., 1993 ). In this study, it was shown a variation of explants browning and total phenols in relation to months of explants collection. The lowest browning percentages were achieved from the explants taken in March, with the highest browning percentages from those collected in June. Higher phenolic levels were associated with higher explants browning but lower survival. It was previously reported that season could an important role in the successful establishment of explants in in-vitro culture ( Dhar & Upreti, 1999 ) and explants survival was inversely related to phenolic content of explants ( Block & Lankes, 1995 ; Dalal et al., 1992 ; Ziv & Halevy, 1983 ). Similarly, higher phenolic content and explants browning were observed with Purbi shoot tips and zygotic embryos while Bedana shoot tips and zygotic embryos showed phenolic contents and better survival.

Time of explants collection is one of the major factors influencing the relative concentration of the various phenolic compounds ( Roussos & Pontikis, 2001a ). In this study, phenolic compounds quantified by HPLC presented significant differences depending on the cultivars and the months. While some of the phenolic compounds including gallic acid, +(−) catechin, catechol and chlorogenic acid showed highly positive correlations with explants browning, rutin exhibited more slightly correlation with the browning. On the other hand, there were not found any correlation between browning and some phenolics such as o-coumeric acid and quercetin. Different quinones produced by different phenolic compounds contribute to a different degree to the formation of the brown color ( Richard-Forget et al., 1992 ). In Olive explants, Roussos and Pontikis, 2001a found significantly positive correlations between some phenolic compounds (luteolin-7-glucoside, quercetin and luteolin) and the browning while they did not found any correlation between browning and some phenolics including rutin, chlorogenic acid and oleuropein.

The concentrations of the different phenolic compounds change during the growing season, presenting the great effect of environmental conditions on the total phenol content of a tissue and especially on individual phenolic compounds ( Lux-Endrich et al., 2000 ). It is well known that the environmental properties, especially temperature and sunlight have important contribution in the formation of the phenolic compounds in plant tissues ( Tangolar et al., 1999 ; Yu & Meredith, 1986 ).

There are a lot of studies conducted on determine the effects of some factors such as genotype, explants origin, season, vigour of litchi and sunlight, on the total phenolic content and explants survival in different plants ( Dalal et al., 1993 ; Fanizza et al., 1984 ; Roussos & Pontikis, 2001a, b ; Tangolar et al., 1999 ; Thomas & Ravindra, 1997 ; Yu & Meredith, 1986 ). But according to our knowledge, variabilities in the individual phenolic compounds of shoot tips and zygotic embryos and their effects on the success of shoot tip and zygotic embryos culture were not previously examined in litchi. We have found that in shoot tips and zygotic embryos of litchi there are important relationships between phenolic compounds and explants browning in the initial stage of cultures. And not only the variation of phenolic compounds but also the percentage of explants browning are related strongly to months of explants collection. So by the careful selection of months browning may be alleviated and thus it is possible to increase the success of shoot tips and zygotic embryos cultures of litchi.