In the xantha1 (xan1) mutant of sunflower (Helianthus annuus L.), the effects on organ anatomy and seedling growth did correlate to the alteration of chloroplast biogenesis. The xan1 seedlings grown under 165 µmol(photon) m-2 s-1 revealed a severely altered chloroplast ultrastructure in cotyledons and leaves. Cross-sections or clarified tissues of the xan1 cotyledons did not show evident alterations with respect to normal cotyledons suggesting that the impairment of chloroplast biogenesis has negligible consequences on embryonic leaves. By contrast, the analysis of xan1 leaves showed that the defects in chloroplast biogenesis were correlated to a drastic reduction of organ size and to a clear enhancement of the trichome growth. The differentiation of palisade and spongy parenchyma in cotyledons and leaves of the xan1 mutant was normal but both organs displayed a drastic reduction in the plastid number with respect to wild type. In addition, xan1 hypocotyls showed a reduced development of the main vascular bundles in comparison with normal seedlings and an undersized central cylinder of the primary root. The exogenous supply of sucrose was not sufficient to revert in vitro the deficit of xan1 growth and the constraints in morphogenetic processes. and M. Fambrini ... [et al.].
Systemic ciliatosis caused by histophagous ciliates constitutes a serious disease of cultured turbot. Six ciliate isolates were obtained from parasitized turbot during six epizootics at four different farms located in Spain, France and Portugal. Axenic cultures of the six isolates were obtained by periodical subculturing in ATCC 1651MA or supplemented L-15 media. In basal media or seawater, the parasites could survive starving for long periods with no apparent proliferation. In adequate media, growth kinetics was found to be very similar for isolates A and B, with a clear influence of temperature. Morphological studies demonstrated that all isolates share common features that allows their assignment to either Philasterides Kahl, 1931 or Miamiensis Thompson et Moewus, 1964. However, statistically significant differences were evident in pairwise comparisons of the isolates from the four farm sites in 16 taxonomically relevant morphometric features. This could allow the discrimination of different species or strains. Virulence of isolates A and B for healthy turbot was tested in several experiments. Differences in the virulence were especially evident after long-term in vitro culturing, isolate A being clearly attenuated after 35-42 passages, whereas isolate B became more virulent after 20-42 passages. The need of further studies to confirm such virulence variability and its implications in pathogenesis and prevention of turbot scuticociliatoses is stressed.
Monitoring some parameters would help to overcome the difficulties that can affect in vitro-grown plants during the crucial step of their acclimatization. Thus, after the determination of net photosynthesis and other parameters during acclimatization of in vitro-grown olive plantlets, we concluded that three months after the transfer to ex vitro, the in vitro-grown olive plants become well acclimated. In fact, even though the net photosynthesis, relatively high in vitro, recorded low values after 15 d from the transfer, it reverted back to its standard rates after 180 d of acclimatization. Transpiration and stomatal conductance first increased significantly with a maximum of 6.22 mmol(H2O) m-2 s-1 and 1.8 mmol(H2O) m-2 s-1, respectively, but they regressed to very low values after 180 d of acclimatization. Some changes in the leaf anatomy were also observed; the reduction of stomata density and inversely, the increase of trichome density, especially on the abaxial side of the leaves, were observed., A. Chaari-Rkhis, M. Maalej, A. Chelli-Chaabouni, L. Fki, N. Drira., and Obsahuje seznam literatury
We studied the relationships between the degree of photoautotrophy, photosynthetic capacity, and extent of photoinhibition of Gardenia jasminoides Ellis plantlets in vitro. Two successive micropropagation stages (shoot multiplication and root induction), and three culture conditions [tube cap closure, photosynthetic photon flux density (PPFD), and sucrose concentration] which may influence the development of photoautotrophy in vitro were assayed. The ratios of variable chlorophyll fluorescence to either maximal (Fv/Fm) or ground (Fv/F0) values were low, irrespective of the culture stage or growing conditions. Incomplete development of the photosynthetic apparatus and permanent photoinhibition may be involved. However, Fv/Fm and Fv/F0 increased from shoot multiplication to root induction owing to a decrease in F0 and an increase in Fm. This suggests that photoinhibition decreases later during micropropagation, when the photoautotrophy of plantlets is more advanced. The low sucrose content and high PPFD increased the photoinhibition of plantlets, whereas growth in tubes with permeable caps showed the opposite effect. The only culture factor with a significant (positive) effect on maximum photosynthetic rate (Pmax) was PPFD. At shoot multiplication net photosynthetic rate (PN) was positively correlated with the half time of the increase from F0 to Fm (t1/2). Such association may be mainly due to a common response of both traits to higher PPFD in culture. Within each culture stage, no relationship was observed between PN and the degree of photoautotrophy, which was positively correlated with Fv/Fm and Fv/F0 during root induction. During shoot multiplication, these correlations were not significant, or were even negative. Hence during the last stage of micropropagation, plantlets with a higher degree of photoautotrophy are less photoinhibited, whereas they do not follow this pattern at the earlier stage. and M. D. Serret ... [et al.].