Novel Phytoplankton Blooms 1989
DOI: 10.1007/978-3-642-75280-3_23
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The Chrysochromulina polylepis Bloom in Scandinavian Waters During Spring 1988

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Cited by 33 publications
(32 citation statements)
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“…Several studies have reported that blooms of toxic phytoplankton species may initiate and develop in natural waters as a result of reduction or absence of grazers due to toxic interactions. For instance, the large bloom of Chrysochromulina polylepis in 1988 in Scandinavian waters has been suggested to develop partly due to reduced grazing (Dahl et al 1989, Maestrini & Granéli 1991. Field observations have shown that Prymnesium parvum are capable of forming more or less monospecific blooms, which may persist in the water for several weeks (Lindholm et al 1999).…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have reported that blooms of toxic phytoplankton species may initiate and develop in natural waters as a result of reduction or absence of grazers due to toxic interactions. For instance, the large bloom of Chrysochromulina polylepis in 1988 in Scandinavian waters has been suggested to develop partly due to reduced grazing (Dahl et al 1989, Maestrini & Granéli 1991. Field observations have shown that Prymnesium parvum are capable of forming more or less monospecific blooms, which may persist in the water for several weeks (Lindholm et al 1999).…”
Section: Discussionmentioning
confidence: 99%
“…have been monitored three times per week in the 0-3 m stratum in Flødevigen Bay, Station 1 (figure 1) by the Institute of Marine Research (Dahl & Johannessen 1998; for the details of sampling and phytoplankton quantification, see Dahl et al 2005). The phytoplankton assemblage sampled in Flødevigen Bay is considered to reflect the abundance in the NCC along the coast (Dahl et al 1989;Dahl & Tangen 1993). The raw timeseries of Chrysochromulina spp.…”
Section: Methodsmentioning
confidence: 99%
“…Details of the isolation by serial dilution and capillary micropipette are described in Krock et al (2008). Subcultures of the original isolate were grown non-axenically at 15-20 C in half-strength K medium (Keller et al, 1987), supplemented with selenite (Dahl et al, 1989), but without addition of ammonium ion. The growth medium was prepared from sterile-filtered (VacuCap 0.2 mm Pall Life Sciences) natural North Sea water (salinity: 32 psu, pH adjusted to 8.0).…”
Section: Isolation and Culture Of The Aza-producing Dinoflagellatementioning
confidence: 99%