Euphausia superba (krill) has been suggested from stomach content analysis (Nemoto 1971(Nemoto /1972) and from the comparison of krill and phytoplankton species distribution (Kawamura 1981). Laboratory experiments can help determine whether krill selectively graze certain phytoplankton species. Graz
Effects of trichlorobenzene on natural phytoplankton populations
β Scribed by N. A. Andresen; L. Sicko-Goad
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 762 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0963-9292
No coin nor oath required. For personal study only.
β¦ Synopsis
Natural phytoplankton assemblages from an offshore station in Lake Michigan were exposed to individual isomers of trichlorobenzene (TCB) and incubated in situ for a 24 h period. One set of exposures was initiated with a lake assemblage collected at 0330 h from 30 m and the TCB isomers added at 0400 h. The second exposure experiment was initiated with an assemblage from 30 m collected at 1530 h and the TCB isomers added at 1600 h.
Comparisons of the chlorophyll a to neutral lipid ratio and the neutral to polar lipid ratios suggest that 1,2,3-TCB is more toxic than 1,2,4-TCB. Furthermore, more effects were observed when exposures were initiated at 0400 h when compared with a parallel experiment initiated at 1600 h. These studies with natural assemblages support culture studies of effect as a function of time of exposure.
π SIMILAR VOLUMES
The cellular fluorescence of chlorophyll a in natural phytoplankton was measured during vertical profiling in marine coastal waters. The ratio of in situ fluorescence to chlorophyll a concentration, which was considered as an index of cellular fluorescence, varied over a wide range, with large chang
Buoyancy of natural populations of marine phytoplankton was studied in a fjord in western Norway during the diatom bloom and in autumn. The study was carried out under approximate in situ conditions by means of an apparatus described in the paper. During the spring bloom, positive buoyancy was obser
A theoretical framework for interpreting flow cytometric histograms from homogeneous phytoplankton populations was developed in part I of this series of articles and applied to chlorophyll fluorescence histograms from clonal cultures in part 11. In this paper, we demonstrate the application of this
Photosynthate incorporation into lipids, low molecular weight compounds, polysaccharides and proteins by individual phytoplankton species isolated from natural populations is described. This sensitive method uses serial solvent extraction and liquid scintillation counting and gives results identical