Brazil has produced 59 t blueberry in 2012, in an area of 270 planted hectares in South and Southeast regions [1] , and the most promising specie for regions of cold weather is the Vaccinium ashei; the species’ cultivars that are better adapted to the Brazilian weather conditions are: Aliceblue, Bluebelle, Bluegem, Briteblue, Climax, Delite, Powderblue, Woodhard [2] . These cultivars are selected from other countries with different edaphoclimatic conditions displaying limitations for its cultivation, which drives the need for superior plants that are able to adapt to Brazil’s particularities [3] . When searching for genetic variability and the development of new cultivars, the propagation of blueberry seeds becomes important [2] .

In order to achieve satisfactory results in seminiferous propagation, it is imperative to know the seed’s germinative behavior and physiologic quality, which can be evaluated through germination and force test, such as the tetrazolium test [4] .

Seed’s germination constitutes of a sequence of physical, biochemical and physiologic events, influenced by a variety of factors, which can act isolated or combined [5] . Those factors can be extrinsic, such as: light, temperature and humidity; and intrinsic, like: morphology, viability and dormancy [6] .

As far as extrinsic factors are concerned, the Vaccinium seeds have its germination affected by temperature [7] and present positive and orthodox photoblastic behavior [8] , meaning it germinates in the presence of light, and is able to maintain the viability even with low humidity content [9] .

In a germination test, the substrate is another extern factor that influences seeds germination, due to its structure, aeration, water retention capacity and level of pathogens infestation [10] . The paper filter is the most utilized support in seeds germination, due to its capacity to simplify the test, increase the speed, and reduce costs [11] . However, the usage of MS medium culture [12] was cited as a substrate for seeds germination of Vaccinium meridionale Swartz since reduction of salts concentration in the culture medium allowed greater percentage of germination [13] .

At the end of a germination test, the presence of non-germinated seeds may occur, because those died, were hard or in dormancy [14] . The seeds dormancy can be classified in: physiological, morphological, physical and combined (physical and physiological) dormancy [15] . The impermeability of the seed coat is a physical dormancy, which prevents the entry of water [16] and can be caused by the presence of substances such as suberin, lignin, cutin, tannins, pectins, as well as derivates of quinine [17] . Chemical studies indicate that the cuticle and pigment chains, present in the seed coat, are composed by insoluble polymeric materials, which can be depolymerized by alkaline hydrolysis [18] with KOH or NaOH [19] .

Viable seeds that are considered in dormancy, present a temporary blockage to complete the germination [20] . The tetrazolium test is a fast method to determinate the viability of the seeds, based on the activity of dehydrogenase enzymes, present in living tissues [21] .

The aim of the present work was to determinate the germinative behavior and levels of the viability of the seeds of Vaccinium ashei Reade cultivars Briteblue and Climax, by germination and tetrazolium tests.

Site and biologic material

Blueberry seedlings from cvs. Climax and Briteblue experimentally planted in spacing of 4.0 m × 1.5 m in 2010, in Ponta Grossa―PR (25˚05'35"S e 50˚03'50"W e 950 m de altitude). The weather is classified as cfb [22] , presenting well-defined dry seasons, frequent frosts during winter and soil Haplic cambisol dystrophic of clay texture, produced the fruits used in the experiments.

Experiment 1―Physiological quality and germinative behavior of Vaccinium ashei Reade seeds, cultivars Briteblue and Climax, treated or not with 5 M of potassium hydroxide (KOH), and submitted to the germination test in different substrates and temperatures

Ripe fruits, collected in February of 2012, were taken to the laboratory, selected, macerated and depulped in order to obtain the seeds. The seeds were washed with running water, spread on paper towels and shade dried at room temperature for 24 hours. Two experiments were performed, one using cv. Briteblue seeds, placed in the refrigerator for two months, and the other with fresh cv. Climax seeds. Furthermore, both cultivars’ seeds were soaked in H₂O (control) or potassium hydroxide solution 5 M (KOH) for 5 minutes, and then submitted to the germination test, installed in Petri dishes, containing the autoclaved substrates: filter paper (SP) periodically moistened with sterile distilled water (2.5 times the weight of the substrate in water) or solid culture medium MS (6 g∙L⁻¹ of agar) with half of salt concentrations (MS/2). Then, the dishes were vetoed with plastic wrap and kept at constant temperatures of 10˚C ± 2˚C (BOD like cabinet) or 25˚C ± 2˚C (climatized room with air conditioning), with photoperiod of 16 hours of light, making the following treatments: T1) Control + SP + 10˚C, T2) Control + SP + 25˚C, T3) Control + MS/2 + 10˚C, T4) Control + MS/2 + 25˚C, T5) KOH + SP + 10˚C, T6) KOH + SP + 25˚C, T7) KOH + MS/2 + 10˚C, T8) KOH + MS/2 + 25˚C. The experimental design was completely randomized with eight treatments, four replicates, and the experimental unit consisted of a Petri dish, containing 10 seeds. The effect of the use of KOH, substrates and temperatures on the germination performance of the seeds was evaluated by the percentage of germination and the first count of normal seedlings (presented all of the essential structures developed). After obtaining the first normal seedling, successive counts were performed every 7 days. The test finished when there was absence of germination after 30 days of test. The percentage data of germination were transformed to arcsen √P%/100, submitted to the Barlett test, followed by analysis of variance, and when significant were compared by Duncan test (p ≤ 0.05), using the SAS statistical package.

Experiment 2―Levels of seeds viability of Vaccinium ashei Reade cultivars Briteblue and Climax through the tetrazolium test

Fruits from cultivars Briteblue and Climax were collected in January of 2013, and were taken to the laboratory and placed under refrigaration. To separate the pulp from the seeds, fruits were placed together with water in a mixer. Next, the seeds were washed with running water, spread on paper towels and shade dried at room temperature for 3 days. To perform the tetrazolium test, three repetitions of 50 seeds were used; 150 seeds in total were pre-wetted by immersion in water for 24 hours, and the exposure of the fabrics to staining were made by a needle in the opposite side of the location of the embryo. Then, the seeds were immersed in a colorless solution of 2,3,4-triphenyl tetrazolium bromide 1% for 3 hours at 30˚C and then kept 21 hours at room temperature in complete darkness condition [8] . After being immersed, the seeds were washed with running water and transversely cut with razor to visualize the embryo [14] in optic microscope (50× increase). The viability was scored by percentage of embryo color (0, 25, 50, 75 and 100%), and stained seeds with embryo above 50% were considered viable.

Experiment 1―Physiological quality and germinative behavior of Vaccinium ashei Reade seeds, cultivars Briteblue and Climax, treated or not with 5 M of potassium hydroxide (KOH), and submitted to the germination test in different substrates and temperatures

The disposal of the treatments T3 and T4 (Briteblue cultivar), and T2, T5 and T6 (Climax cultivar) was due to a contamination of the substrate by fungus. This interfered de evaluation of the factors: exposition or not to potassium hydroxide (KOH), substrates (SP and MS/2) and temperatures (10˚C and 25˚C) in factorial arrangement 2 × 2 × 2.

Table 1 shows the results of analysis of variance of germination percentage transformed to arcsin √P%/100, and the value of chi-square (c²) for the Barlett test, which showed homogeneity of variances of treatments.

For the germination test of blueberry seeds of Briteblue cultivar, in the treatments T1 and T2, which contained seeds immersed in water for 5 minutes and germinated on paper, had germination percentages of 30% and 40% respectively, yet they did not differ significantly as a function of temperature (10˚C and 25˚C). To the T6 and T8

^*significant at 5% of probability.

treatments, which contained seeds, treated with 5M of KOH and were germinated at a temperature of 25˚C, had germination percentages of 7% and 10% respectively; these did not differ significantly in relation with the substrate (SP and MS/2).

The T2 treatment revealed to be statistically superior to the T6 treatment, showing that the exposure of the seeds to 5m of KOH inhibited the germination in relation with the seeds that were only immersed in water and germinated on paper at the same temperature (Figure 1).

For the Climax cultivar, the T1 and T4 treatments, presented the best statistical performance and germination percentages of 40% and 30% respectively, surpassing the other treatments. The T7 treatment, which had seeds treated with 5M of KOH and was germinated on the substrate MS/2 at 25˚C, presented inferior statistical results than the other treatments, and germination percentage of 5% (Figure 2).

The first detached normal seedling was obtained after 46 days to Climax cv. treatment T8 (KOH + MS/2 + 25˚C) and after 52 days to Briteblue cv. on treatment T5 (KOH + SP + 10˚C). Seeds of Vaccinium meridionale Swartz, stored for a week in ambient conditions at a temperature of 18˚C ± 2˚C, using as substrate the culture medium MS with 1/3, 1/8 and 1/16 of the salt concentration, initiated the germination 42 days post the test installation [13] .

The germination test of the seeds of Vaccinium ashei Reade Briteblue and Climax cultivars was terminated after 6 months of its installation, when the absence of germination was superior to 30 days. Evidence of dor-

mancy in seeds of Vaccinium spp. are often manifested by the low and irregular germination, as observed in V. angustifolium, V. ashei, V. canadense, V. corymbosum, V. macrocarpon and V. oxycoccus [23] . In wild oat dormant seeds the use of KOH promoted significantly improvement on the germination [19] . Similarly seeds of Vaccinium angustifolium Ait. had maximum germination (approximately 80%) when treated with 5.3 M of KOH for 5 minutes [24] ; results that were not seen in the tested cultivars of this study, showing that within the same genus, species have different behavior regarding KOH usage.

The usage of paper filter as a substrate has been observed in the seeds germination of Vaccinium membranaceum [25] , Vaccinium arctostaphylos L. [26] and Vaccinium parvifolium Smith [7] . On the other hand, the culture medium MS with 1/3, 1/8 and 1/16 of the original salt concentration has been tested as a substrate [13] in the seeds germination of Vaccinium meridionale. Promoting germination percentages of 48, 63, 63.5% respectively. In the present experiment both substrates, SP and MS/2, promoted seeds germination of the Vaccinium ashei Reade for both tested cultivars.

Many temperature schemes can affect the germination of Vaccinium sp [7] , fact that can be observed over the different temperatures used for germination of seeds of this genus. In order to simulate Canadian typical spring conditions, seeds of Vaccinium angustifolium Ait. were germinated at 10˚C [24] . On the other hand, when working with Vaccinium myrtillus L. and Vaccinium vitis-idaea, obtained germination of 62% - 100% in presence of light and alternate temperatures of 20:10˚C [27] . In the present study both constant temperatures of 10˚C ± 2˚C (BOD) and 25˚C ± 2˚C (SC) enabled the germination of Vaccinium ashei Reade seeds, although Climax cultivar, when variables were maintained constant, using or not KOH and substrate, at 25˚C, showed germination percentage statistically superior than the one at 10˚C.

Experiment 2―Levels of seeds viability of Vaccinium ashei Reade cultivars Briteblue and Climax through thetetrazolium test

In order to obtain satisfactory results in the tetrazolium test, is required that the 2,3,5, triphenil tetrazolium bromide solution is absorbed by the seeds. Thus, some species need preparation steps, such as puncture, cut and/or removal of the seed coat [21] . The puncture of the seed coat with a needle was essential so that the tetrazolium solution was able to act inside the seed, demonstrating impermeability by the tested cultivars. The class levels established in the tetrazolium test for the Briteblue and Climax cvs. seeds are represented in percentage staining red-orange of the embryo (Figure 3 and Figure 4). Embryos Vaccinium meridionale Swartz, treated with tetrazolium solution at 1%, showed staining from light pink to dark pink, with shades of Orange [8] . Embryos with less than 50% of staining red-orange were considered not viable. The number of classes depends on the seed staining, morphological characteristics of the specie, and on the applied treatments, and for different species, distinct levels of classes can be proposed [28] .

Accordingly with the levels of proposed classes, to Briteblue cv., were considered viable the seeds that presented 50%, 75% and 100% of staining red-orange of the embryo (Figures 3(d)-(f)), which represent respectively

13%, 7% and 9% of the evaluated seeds (Figure 5(a)). Seeds that showed red-orange embryo staining of approximately 25% (Figure 3(c)) corresponded to 20% of the sample and were not considered viable, as well as those that were not stained (dead or 0% of red-orange staining―(Figure 3(a) and Figure 3(b)), which repre- sented 51% of the sample (Figure 3(a)), and from this percentage dead seeds correspond to 46%.

The same viability standards used to analyze the Briteblue cv. results, which were also used for Climax cv., were considered viable for the seeds that presented 50%, 75% and 100% of embryo staining red-orange (Figures 4(d)-(f)) and that represented respectively 8%, 13.5% and 28.5% of the sample (Figure 4(b)). Seeds that showed red-orange embryo staining of approximately 25% (Figure 4(c)) corresponded to 19% of the sample and were not considered viable. Those that were not stained (0% of red-orange staining or dead) represented 31% of the sample (Figure 5(b)).

Adding the percentage of the seeds that had the embryo stained red-orange over 50% in the tetrazolium test, 29% of the Briteblue cv. seeds and 50% of the Climax cv. seeds were considered viable. Vaccinium meridionale Swartz submitted to the tetrazolium test showed 84.2% of viability, and from those, 63% germinated and 21.2% did not germinate (remained dormant) [8] . The low percentage of germination of seeds can be related to elevated number of unviable seeds in the tetrazolium test, or viables that remained in latent state.

Briteblue and Climax cvs. of blueberry seeds, which were pre-treated with 5 M of KOH for 5 minutes and germi-

nated on the same substrate at the same temperature, had low germination percentage in relation with the non- treated seeds.

Blueberry seeds of both tested cultivars had their germinative behavior altered when the variables temperature (10˚C and 25˚C) and substrate (SP and MS/2) were combined.

Vaccinium ashei Reade blueberry seeds treated with combination of the variables: exposure or not to KOH, substrates (SP and MS/2) and temperature (10˚C and 25˚C) required up to 46 days to emit the first normal seedling and showed slow germination, and after 6 months of beginning the germination test, germination percentage dose did not exceed 40%.

The tetrazolium test, based on the staining of the fabrics, allows the establishment of different levels of viability, which is valuable for blueberry seeds.

Research support by CAPES, ARAUCÁRIA FOUNDATION, and UEPG.

Ana Paula deAzevedo Pasqualini,Jessé Nevesdos Santos,Ricardo AntonioAyub, (2016) Behavior and Viability of Blueberry Seeds through Germination and Tetrazolium Test. Advances in Bioscience and Biotechnology,07,11-18. doi: 10.4236/abb.2016.71002