Effects of temperature, salinity and irradiance on the growth of the harmful red tide dinoflagellate Cochlodinium polykrikoides Margalef (Dinophyceae)

By Dae-Il Kim, Y. Matsuyama, Sou Nagasoe, M. Yamaguchi, Y. Yoon, Y. Oshima, N. Imada, T. Honjo. 2004

220 citations recorded by the source corpus.

Subfields: Environmental Chemistry, Oceanography

View Paper: https://www.semanticscholar.org/paper/4a63779db8f42bb3bdcaf390fd6a50f384de944e

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In Environmental Chemistry

1. Raphael M. Kudela
2. C. Gobler
3. T. Smayda
4. Y. Collos
5. I. Imai
6. M. Yamaguchi
7. E. Masseret
8. H. Jeong

In Oceanography

1. C. Gobler
2. Raphael M. Kudela
3. T. Smayda
4. H. Jeong
5. Y. Collos
6. Y. Yoo
7. A. Vaquer
8. K. Seong

Citations in the corpus

• Control of the harmful alga Cochlodinium polykrikoides by the naked ciliate Strombidinopsis jeokjo in mesocosm enclosures (2008, background): “Blooms of C. polykrikoides have recently been observed in several other countries, including China (Huang and Dong, 2000), Russia (Vershinin et al., 2005), and Japan (summarized by Kim et al., 2004), and have also led to considerable losses for their aquaculture industries.”
• First occurrence of Cochlodinium blooms in Sabah, Malaysia (2008, background): “The temperature and salinity tolerances for growth of this dinoflagellate were 15–30 8C and 20–36 psu, respectively (Kim et al., 2004).”
• A hierarchy of conceptual models of red-tide generation: Nutrition, behavior, and biological interactions (2015, unknown): “002 MA Kim et al. (2013)”
• Influence of temperature, salinity and irradiance on the growth and cell yield of the harmful red tide dinoflagellate Alexandrium catenella colonizing Mediterranean waters (2011, methodology): “Irradiance is also an important environmental factor that influences physiological reactions in microalgae; growth rate can be reduced under low irradiance, and photoinhibition can occur at a high light intensity (Kim et al., 2004; Baek et al., 2008).”
• Light as a driver of phytoplankton growth and production in the freshwater tidal zone of a turbid estuary (2011, background): “Dinoflagellates are usually described as “shade” species (Raven and Richardson, 1986) and saturating irradiances for several dinoflagellate species grown in cultures vary between 70 and 114 mmol photonsm 2 s 1 (Yamaguchi et al., 1997; Kim et al., 2004; Nagasoe et al., 2006; Matsubara et al., 2007).”
• Eutrophication and occurrences of harmful algal blooms in the Seto Inland Sea, Japan (2006, background): “The growth response of C. polykrikoides was examined in different combinations of temperature and salinity (Kim et al. 2004, Yamatogi et al. 2005, 2006).”
• Complexity in the eutrophication–harmful algal bloom relationship, with comment on the importance of grazing (2008, methodology): “The relationship between growth rate, m, and irradiance follows a similar geometry, and can be modeled using the equation that Kim et al. (2004) applied to Cochlodinium polykrikoides: m ¼ mm½I Io=I þ ðIk 2Io (3) where m is the specific growth rate (day 1), mm is the maximum specific growth rate…”
• Characterization, dynamics, and ecological impacts of harmful Cochlodinium polykrikoides blooms on eastern Long Island, NY, USA (2008, unknown): “polykrikoides grows optimally (21 and 26 8C), although the decline in temperature during late August and September from 25 8C to below 20 8C may have contributed to the bloom’s demise (Table 1; Kim et al., 2004; Yamatogi et al., 2006).”
• Harmful dinoflagellate blooms caused by Cochlodinium sp.: Global expansion and ecological strategies facilitating bloom formation (2012, background): “2 to 45 mmol photons m 2 s 1 (Kim et al., 2004; Yamatogi et al., 2005; Oh et al., 2006) for C.”