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Culture of Spirogyra africana from farm ponds for long- term ...

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426 Biotechnol. Agron. Soc. Environ. 2013 17(3), 423-430 Gallego I., Casas J.J., Fuentes-Rodriguez F. et al.and number <strong>of</strong> rhizoids per filament. When ANOVAsshowed significant differences between groups (culturemedia, chlorination conditions), Tukey’s HSD posthoctests were used. All analyses were per<strong>for</strong>med withSTATISTICA 7.1 s<strong>of</strong>tware (Stats<strong>of</strong>t Inc., 2005).a0.040.02b3. RESULTS3.1. Effect <strong>of</strong> culture media on S. <strong>africana</strong> growthrateThe three culture media showed substantial differencesin nutrient composition (Table 1). HSCHU#10 andsD11 contained N:P molar ratios that varied <strong>from</strong> aP-impoverished FPW medium to a N-depleted ratioin sD11, whereas HSCHU#10 showed an N:P rationearest to the optimal Redfield ratio <strong>for</strong> phytoplankton,namely 16:1.At the end <strong>of</strong> the experiment, S. <strong>africana</strong> onlyshowed a positive growth rate in HSCHU#10(Figure 1). All replicates in sD11 and FPW showednegative growth rates. The two-factor ANOVA testshowed significant differences in S. <strong>africana</strong> growthrate between culture media (F = 429.784; P < 0.001),between chlorination treatments (F = 152.025;P < 0.001) and in the interaction <strong>of</strong> both factors(F = 53.315; P < 0.001).Table 1. Nutrient concentration (mg.l -1 ), N:P molar ratioand pH <strong>of</strong> the three culture media tested to de<strong>term</strong>ineits effect on growth, filament survival and rhizoiddevelopment <strong>of</strong> <strong>Spirogyra</strong> <strong>africana</strong> — Concentration deséléments nutritifs (mg.l -1 ), rapport molaire N:P et ph destrois milieux de culture testés pour dé<strong>term</strong>iner son effet surla croissance, la survie des filaments et le développementdes rhizomes de <strong>Spirogyra</strong> <strong>africana</strong>.ParameterMediumHSCHU#10 sD11 FPWCa 2+ 4.89 16.98 221.52Mg 2+ 1.23 9.86 130.07Fe 3+ 0.14 1.00 n.m.K + 0.56 41.54 30.02Na + 4.52 13.84 330.55Cl - 0.09 7.13 472.75NO 3- 7.56 26.26 1.27PO 43-1.36 81.78 0.001HCO 3-+ CO 32-5.66 21.43 48.3N:P molar 8.5:1 1:2 1088:1pH 7.3 7.1 8.4n.m. = not measured value — valeur non mesurée.Growth rate (d -1 )0.00-0.02-0.04-0.06-0.08HSCHU#10sD11FPWHSCHU#10sD11FPWFigure 1. Growth rate (expressed as d -1 ) <strong>of</strong> <strong>Spirogyra</strong><strong>africana</strong> in three culture media tested, in non-chlorinated(a) and chlorinated samples (b) — Taux de croissance (parjour) de <strong>Spirogyra</strong> <strong>africana</strong> dans trois milieux de culturetestés, dans des échantillons non chlorés (a) et chlorés (b).Bars denote standard error — Les barres indiquent l’erreurstandard; *** P < 0.001: two-way ANOVA — ANOVA à deuxfacteurs.3.2. Effect <strong>of</strong> culture media on live filamentsThe type <strong>of</strong> culture media also affected the percentage<strong>of</strong> live filaments (ANOVA F = 150.093; P < 0.001),with HSCHU#10 proving to be the highest and FPWthe lowest (Figure 2). Furthermore, the effect <strong>of</strong> culturemedia and time was significant (ANOVA F = 53.452;P < 0.001), since HSCHU#10 showed asymptoticvalues around 90% <strong>of</strong> the initial value after 10 weeksand both sD11 and FPW showed percentages close to40% at the end <strong>of</strong> the experiment. Chlorination hadno effect on the percentage <strong>of</strong> live filaments (ANOVAF = 2.665; P > 0.05) but the interaction <strong>of</strong> time andchlorination showed a positive effect (ANOVAF = 19.019; P < 0.001).3.3. Effect <strong>of</strong> culture media on rhizoid productionRhizoid genesis was observed <strong>from</strong> the first week afterinoculation (Figure 3). The percentage <strong>of</strong> rhizoids perlive filament was affected by the type <strong>of</strong> culture mediaused (ANOVA F = 4.044; P < 0.05). Tukey’s HSDpost hoc test showed that sD11 was the medium with

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