2002
DOI: 10.1016/s0377-8398(01)00040-8
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Techniques for quantitative analyses of calcareous marine phytoplankton

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Cited by 79 publications
(55 citation statements)
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“…Additionally, samples can be prepared for light microscopy either by filtration or by using the Utermöhl sedimentation method (Utermöhl, 1958). Reid (1980) and Bollmann et al (2002) both concluded that inverted light microscopy is unreliable for determining cell densities of small coccolithophores.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Additionally, samples can be prepared for light microscopy either by filtration or by using the Utermöhl sedimentation method (Utermöhl, 1958). Reid (1980) and Bollmann et al (2002) both concluded that inverted light microscopy is unreliable for determining cell densities of small coccolithophores.…”
Section: Discussionmentioning
confidence: 99%
“…Cell counts from SEM can additionally be unreliable at high cell densities, where shedded coccoliths can lead to difficulties in distinguishing individual coccospheres (A. Poulton, personal observation). The synthesis of datasets obtained from these different methods would be greatly improved by further comparative studies similar to those carried out by Bollmann et al (2002), as it is currently unclear to what extent small and rare species are being overlooked in different ocean regions as a result of these methodological differences.…”
Section: Discussionmentioning
confidence: 99%
“…The samples were investigated using a Motic Polarizing Microscope (PM, BA300) under 1000 × magnification with more than 300 coccoliths or 100 coccospheres being identified and counted per filter according to Heimdal (1997), Bollmann et al (2002), Yang et al (2003), Jordan et al (2004) and Frada et al (2010). Coccolith/coccosphere abundance was calculated following the method described in Sun et al (2011) as the following equation:…”
Section: Coccolith and Coccosphere Data Analysis And Statistical Methodsmentioning
confidence: 99%
“…The qualitative microscopic screening was performed to verify the presence of the dominant phytoplankton groups in conjunction with specific pigment biomarkers (Havskum et al, 2004;Irigoien et al, 2004). Sea surface water samples (1.0 l) for scanning electron microscopy (SEM) were filtered through polycarbonate membrane filters (0.8 lm pore size, Ø 47 mm, Millipore), dried onboard for 12 h at 50°C and stored dry before being mounted onto microscope slides and coated with gold (Bollmann et al, 2002). Coccolithophores were identified by scanning electron microscopy (SEM) using a Jeol JSM 5600 LV at a minimum magnification of 600 times.…”
Section: Microscopic Phytoplankton Identificationmentioning
confidence: 99%