Biomass
Under non-stressful conditions, the high biomass of an average of 43.82 g was noted in genotype S (Table 1). We notice a natural aging effect in the three genotypes S, M and SW which record low values compared to the control under favorable conditions, with minimum of 17.54 g recorded in genotype SW and a maximum of 19.97 noted in genotype S and a more important decrease in variety M under unfavorable conditions with 11.99 g (Fig 1). Variety B was not affected by natural aging under both conditions.
The statistical analysis of the variance of the results obtained between the natural aging conditions shows that there are no significant differences; the same result is obtained for the factor variety and for the interaction of the two factors (variety × natural aging).
The relative water content (RWC %)
A comparison between the evolutions of the moisture content of the four wheat varieties studied showed that the relative moisture content decreases as the natural aging conditions become difficult. The highest moisture contents are noted in the controls, with a maximum value of (95.69) recorded in genotype B (Table 2) and a minimum value of (93.22) recorded in genotype S (Fig 2). In contrast, the lowest water contents are recorded for the unfavorable conditions of natural aging in the four genotypes studied. The analysis of variance at the factor of Natural aging gives a very highly significant difference. The results obtained at the factor variety and at the factor interaction (variety × natural aging) are not significant.
Variation in total protein content (μg/100 mg MF)
Under non-stressful conditions, an accumulation of soluble proteins averaging 49.06 to 43.11 μg/100 mg MF was noted in the two genotypes M and B respectively (Fig 3). We notice a natural aging effect in the four genotypes B, S, M and SW which record low values compared to the control under both conditions (favorable, unfavorable) with a minimum of 19.82 g recorded in the SW genotype and a maximum of 21.22 g noted in the B genotype (Table 3); while there is no difference between the two NA conditions. The statistical analysis of the variance of the results obtained reveals the existence of a very highly significant difference between the NA conditions and a highly significant difference in the interaction of the two factors (variety × natural aging). While for the variety factor the differences are not significant.
Variation in proline content (μg/100 mg MF)
Under non-stress conditions, proline accumulation averaging 11.54 to 27.7 μg/100 mg MF was noted in the two genotypes M and B respectively (Fig 4).
A significant increase in the proline level of seeds subjected to NA vs. compared to the control which recorded high proline values under both conditions of NA. The contents increase more significantly under unfavorable conditions in the two genotypes B and M with 52.5 genotypes B and M with 52.07 and 31.74 respectively (Table 4).
The statistical analysis of the variance of the results obtained shows that the non-significant differences significant differences between the NA conditions and for the variety factor; as well as for the interaction of the two factors (variety × natural aging).
Variation in soluble sugar content (ìg/100 mg MF)
Under good natural aging conditions, we notice that the different genotypes tested record low soluble sugar contents compared to the control, with a maximum of 9.49 μg/100 mg MF recorded in the Bousellam genotype and a minimum of 6.95 μg/100 mg noted in the Setifis genotype (Fig 5).
Under unfavorable NA conditions, a significant increase in soluble sugar content is noted which is estimated with a minimum of 12.33 μg/100 mg MF in S and The M genotype mentions the maximum content of 16.06 μg/100 mg MF (Table 5).
The statistical analysis of the variance of the results obtained reveals the existence of a very highly significant difference between the natural aging conditions and a highly significant difference for the variety factor. While for the interaction of the two factors (variety × natural aging), the differences are not significant.
In light of the results obtained during our study, we found a decrease in germination rate according to the duration and conditions of storage for all the varieties studied. We found that seeds stored under unfavorable conditions are the most affected; they represent lower germination rates compared to seeds stored under favorable conditions.
According to
Multon (1982), storage time is a factor that amplifies deterioration phenomena. Thus,
Booth et al., (2001) and
Srivastava, (2002) believe that the lower germination of aged seeds is due to the natural aging process, even when stored under controlled temperature and humidity conditions the seeds gradually lose their viability. If the humidity balance between the seeds and the ambient air leads to an increase in seed humidity, the deterioration process increases with the concomitant temperature inside the seeds, resulting in a decrease in germination and vigor.
Our results are in agreement with many works that report a reduction in germination capacity after long storage periods under unfavorable conditions (
Govender, 2008). Other studies have shown that germination has a negative correlation with temperature and storage period in many species such as;
Phaseolus vulgaris (Rani et al., 2013), Hordeum vulgare and
Avena sativa L.
(White et al., 1999), Triticum durum
(Karunakaran et al., 2001, Nithya et al., 2011) and
Secale cereale L.
(Sathya et al., 2008, 2009).
The increase in the content of reducing sugars in the four wheat varieties studied would be the result of increased degradation of the starch during treatment. These sugars would initiate Amadori and Maillard reactions
(Callucci et al., 2004; Sun and Leopold, 1995) responsible for the browning of the grains and especially associated with the loss of viability during storage. The decrease in protein levels observed in stored seeds may be the consequence of the formation of free radicals that will denature, oxidize, or degrade these proteins to form carbonyl derivatives (
Alayat, 2015). Quantification of proline was performed on the leaves of wheat seedlings. The results show a very significant increase in proline content in the leaves of seedlings from old seeds in all varieties studied.
The decrease in protein content, along with the increase in proline and soluble sugar content in the four varieties studied would be part of the overall biochemical degradation that grains would undergo during storage. These same changes were observed in peas (
Kalpana and Rao, 1994) and wheat seeds
(Krishnan et al., 2003) artificially aged.
The degradation of soluble proteins would affect in particular gliadins and glutenins whose role in bread-making quality is no longer to be demonstrated. The increase in proline content during accelerated aging could be explained as a consequence of protein degradation or simply as a response to the heat stress (40°C) that the seeds undergo during processing.
Draw attention to the use of relative water content as an indicator of plant water status under stress (
Chaffai, 2013). The results regarding this parameter show a very slight and non-significant decrease with storage time in all varieties studied. The study of the RWC of plant leaves is used as an indirect selection criterion in genetic improvement for varieties (
Douib, 2012). However, this test is applied much more to estimate the tolerance of plants to water or salt stress. It is related to the ability of the plant to maintain a level of tissue hydration (
Aoumeur, 2012).