2012
DOI: 10.1111/j.1529-8817.2012.01185.x
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EXTREMELY HIGH GROWTH RATE OF THE SMALL DIATOM CHAETOCEROS SALSUGINEUM ISOLATED FROM AN ESTUARY IN THE EASTERN SETO INLAND SEA, JAPAN1

Abstract: Small single-celled Chaetoceros sp. are often widely distributed, but frequently overlooked. An estuarine diatom with an extremely high growth potential under optimal conditions was isolated from the Shinkawa-Kasugagawa estuary in the eastern part of the Seto Inland Sea, western Japan. It was identified as Chaetoceros salsugineum based on morphological observations. This strain had a specific growth rate of 0.54 h(-1) at 30°C under 700 μmol · m(-2)  · s(-1) (about 30% of natural maximal summer light) with a 14… Show more

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Cited by 24 publications
(14 citation statements)
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References 23 publications
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“…In vivo fluorescence was used as a proxy for photosynthetic biomass, because it allowed efficient daily measurements of a large number of simultaneously maintained cultures (as many as 90 at a time). All well-acclimated replicates were kept in the same nutrient conditions, and growth rates were calculated from in-vivo fluorescence of each individual replicate measured relative to itself over time (9,(18)(19)(20)(21). Although In-vivo fluorescence was never used to compare biomass across different light and temperature treatments, in a pilot study we observed that fluorescence and cell counts increased linearly even across different light and temperature treatments ( Figure S1).…”
Section: Temperature and Light Assaysmentioning
confidence: 99%
“…In vivo fluorescence was used as a proxy for photosynthetic biomass, because it allowed efficient daily measurements of a large number of simultaneously maintained cultures (as many as 90 at a time). All well-acclimated replicates were kept in the same nutrient conditions, and growth rates were calculated from in-vivo fluorescence of each individual replicate measured relative to itself over time (9,(18)(19)(20)(21). Although In-vivo fluorescence was never used to compare biomass across different light and temperature treatments, in a pilot study we observed that fluorescence and cell counts increased linearly even across different light and temperature treatments ( Figure S1).…”
Section: Temperature and Light Assaysmentioning
confidence: 99%
“…Hence, the time-effective aspect of the microplate-based assay would no longer be an advantage compared with culture flasks. As a linear relationship exists between chlorophyll fluorescence and cell density in steady experimental conditions (Ichimi et al, 2012), using either of these methods should not bias the growth rate calculation. However, this is only true when chlorophyll fluorescence of individual microalgal cells is not modified by the substance they are exposed to, relative to the control culture.…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…The longer the time required for plant growth, the less efficient is the plant’s ability to utilize the total available solar energy and land area during its life cycle. A diatom like Chaetoceros has a very short growth cycle [34]. Under sub-tropical conditions as mentioned above, Wang and his group have demonstrated (unpublished work) that using 20% of the diatoms produced during the previous day as seed inoculum, their growth test systems (see Fig.…”
Section: Production and Harvestingmentioning
confidence: 99%