ICES Zooplankton Methodology Manual 2000
DOI: 10.1016/b978-012327645-2/50009-8
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Cited by 149 publications
(143 citation statements)
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“…The trophic interactions are particularly complex in subtropical coastal and estuarine environments where planktonic abundances, compositions and mesozooplankton feeding preferences are temporally variable because of dynamic hydrographic conditions (Gifford et al, 2007 and this study). Factors that regulating the feeding rates of mesozooplankton in dynamic environments generally include abundance of food items that affects the functional response of grazers, prey particle size and palatability that affects the feeding selectivity of grazers, characteristics of grazers (size and feeding behavior), physical environmental parameters (temperature and salinity) and turbulence (Kiørboe and Saiz, 1995;Båmstedt et al, 2000;Levinsen et al, 2000). Our result showed that mesozooplankton clearance rate (feeding rates per biomass) was FIGURE 8 | Mesozooplankton clearance rates on total phytoplankton community (Total) and phytoplankton with different sizes (Large: >20 µm; Middle: 2 ∼ 20 µm and 5 ∼ 20 µm in the first and the second sampling year, respectively; Small: <2 and <5 µm in the first and the second sampling year, respectively) at the two stations EO and WE.…”
Section: Discussion the Net Effect Of Mesozooplankton Feeding On Phytmentioning
confidence: 99%
“…The trophic interactions are particularly complex in subtropical coastal and estuarine environments where planktonic abundances, compositions and mesozooplankton feeding preferences are temporally variable because of dynamic hydrographic conditions (Gifford et al, 2007 and this study). Factors that regulating the feeding rates of mesozooplankton in dynamic environments generally include abundance of food items that affects the functional response of grazers, prey particle size and palatability that affects the feeding selectivity of grazers, characteristics of grazers (size and feeding behavior), physical environmental parameters (temperature and salinity) and turbulence (Kiørboe and Saiz, 1995;Båmstedt et al, 2000;Levinsen et al, 2000). Our result showed that mesozooplankton clearance rate (feeding rates per biomass) was FIGURE 8 | Mesozooplankton clearance rates on total phytoplankton community (Total) and phytoplankton with different sizes (Large: >20 µm; Middle: 2 ∼ 20 µm and 5 ∼ 20 µm in the first and the second sampling year, respectively; Small: <2 and <5 µm in the first and the second sampling year, respectively) at the two stations EO and WE.…”
Section: Discussion the Net Effect Of Mesozooplankton Feeding On Phytmentioning
confidence: 99%
“…Zooplankton grazing rates were not measured during the present study. However, the mesozooplankton ingestion rate (I ) can be estimated from the fecal pellet sinking rate measured at 150 m (E ), assuming an assimilation efficiency (AE) of 70% (Carlotti et al 2000) and using the relationship I = E / (1 -AE) (Båmstedt et al 2000). This calculation gives potential ingestion rates of 147, 87 and 177 mg C m -2 d -1 by the migrating zooplankton population in the upper water column on Days 2, 4 and 6, respectively.…”
Section: Mesozooplankton Grazing In the Upper Twilight Zonementioning
confidence: 99%
“…Copepod or fecal pellets were sampled directly into extraction tubes. When more time is needed to sort samples of live animals after washing, they should be rapidly frozen before sorting as described by Båmstedt et al (2000). Copepods were subfractioned for subsequent pigment and DNA analysis.…”
Section: Materials and Proceduresmentioning
confidence: 99%
“…In order to quantify the trophic interactions of copepods and other mesozooplankton in situ, it is not only necessary to assess all important prey, including heterotrophs, but it should also be done with an absolute minimum of handling and temporal and spatial confinement prior to collection and analysis of the predator. Several methods have been developed to assess mesozooplankton grazing rates (Båmstedt et al 2000), including the fast and coarse gut pigment method (Mackas and Bohrer 1976), isotope-based in vitro approaches (Roman and Rublee 1981), and laborious time-intensive microscopy-based studies (Verity and Paffenhöfer 1996;Nejstgaard et al 2001). Each approach has its own experimental limitations.…”
mentioning
confidence: 99%