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Optimization of a high-throughput phenotyping method for chain-forming phytoplankton species

Gross, Susanna, 1982 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences
Kourtchenko, Olga, 1980 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences
Rajala, Tuomas, 1981 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för matematiska vetenskaper,Department of Mathematical Sciences
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Andersson, Björn, 1985 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences
Fernandez Ricaud, Luciano Francisco, 1975 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences
Blomberg, Anders, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology
Godhe, Anna, 1967 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för marina vetenskaper,Department of marine sciences
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 (creator_code:org_t)
2017-11-27
2018
Engelska.
Ingår i: Limnology and Oceanography : Methods. - : Wiley. - 1541-5856. ; 16:2, s. 57-67
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Modern equipment facilitates phenotyping of hundreds of strains of unicellular organisms by culturing and monitoring growth in microplates. However, in the field of phytoplankton ecology, automated monitoring of growth is not often done and this method has not been tested for many species. To meet the demand for a high-throughput technique for monitoring growth of chain-forming phytoplankton species, we have assessed and optimized a method commonly used for other microorganisms. Skeletonema marinoi is a pelagic chain-forming diatom, and we have acquired growth patterns in four different treatments (i.e., low and high light, low and high nutrient concentrations) when cultured in multi-well plates. Due to the unexpected heterogeneity in growth rates and maximum cell densities observed between wells (spatial) and runs (temporal), a set of models was fitted to the obtained phenotypic data to correct for these biases. Models were tested for robustness on two replicate multi-strain experiments including 23 different strains. Using the model accounting for temporal and spatial bias, we could reliably determine changes in growth rate caused by nutrient treatments as well as differences in cell density as a response to nutrient availability and light treatment. This method can facilitate high-throughput phenotyping of hundreds of strains, which is often a bottleneck in characterizing the ecology and capacity for adaptation of chain-forming phytoplankton.

Ämnesord

NATURVETENSKAP  -- Biologi -- Mikrobiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Microbiology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Ekologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Ecology (hsv//eng)

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