2018
DOI: 10.1080/09670262.2018.1458997
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Biostimulant activity of humic-like substances from agro-industrial waste onChlorella vulgarisandScenedesmus quadricauda

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Cited by 44 publications
(36 citation statements)
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“…Microalgal growth was conducted in 250 mL flask containing 150 mL of sterile BG11 culture medium [ 37 ] at pH 8.4, incubated on a mechanical shaker (100 rpm) at 25–30 °C, illuminated by a 3500-lx, average photon flux (PPF) 100 μmol photons m −2 s −1 light source (PHILIPS SON-T AGRO 400) with a 12 h photoperiod for 30 days in a growth chamber and aerated by pumps with 20 L h –1 1.5% CO 2 [ 38 ]. Microalgal biomasses were harvested by centrifugation (at 5000 rpm for 15 min), washed with distilled water (up conductivity < 200 μS cm −1 ), and freeze-dried as described in Puglisi et al [ 39 ].…”
Section: Methodsmentioning
confidence: 99%
“…Microalgal growth was conducted in 250 mL flask containing 150 mL of sterile BG11 culture medium [ 37 ] at pH 8.4, incubated on a mechanical shaker (100 rpm) at 25–30 °C, illuminated by a 3500-lx, average photon flux (PPF) 100 μmol photons m −2 s −1 light source (PHILIPS SON-T AGRO 400) with a 12 h photoperiod for 30 days in a growth chamber and aerated by pumps with 20 L h –1 1.5% CO 2 [ 38 ]. Microalgal biomasses were harvested by centrifugation (at 5000 rpm for 15 min), washed with distilled water (up conductivity < 200 μS cm −1 ), and freeze-dried as described in Puglisi et al [ 39 ].…”
Section: Methodsmentioning
confidence: 99%
“…Chlorella vulgaris (CCAP 211/11C) was obtained and maintained in the algal collection of the Department of Agriculture, Food and Environment (Di3A) (University of Catania, Catania, Italy). C. vulgaris was cultivated as detailed in Puglisi et al [22]. Briefly, microalgae were grown in standard BG11 algae culture medium in a growth chamber, bubbled with air using a pump at around 180 bubbles per minute through a plastic tube fitted to an air regulator, illuminated by a 3500-lux, average photon flux (PPF) 100 µmol m −2 s −1 light source (SON-T AGRO 400, PHILIPS, Eindhoven, the Netherlands), with a 12 h photoperiod (microphotography image is provided in Supplementary Figure S1).…”
Section: Microalgae Culture and Extract Preparationmentioning
confidence: 99%
“…The microalgae was cultivated in a growth chamber using standard BG11 algae culture medium [33] bubbled with air and illuminated by a 3500-lux, average photon flux (PPF) 100 µmol m −2 s −1 light source (PHILIPS SON-T AGRO 400) with a 12 h photoperiod [34]. The biomass was obtained by centrifugation and the pellet was washed more times with distilled water to reach a conductivity <200 µS cm −1 [35].…”
Section: Microalgae Culture and Extract Preparationmentioning
confidence: 99%