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A significant seasonal variation in size at settlement has been observed in newly settled larvae of Dreissena polymorpha in Lake Constance. Diet quality, which varies temporally and spatially in freshwater habitats, has been suggested as a significant factor influencing the life history and development of freshwater invertebrates. Accordingly, experiments were conducted with field-collected larvae to test the proposal that diet quality can determine planktonic larval growth rates, size at settlement and subsequent post-metamorphic growth rates. Larvae were fed one of two diets or starved. One diet was composed of cyanobacterial cells, which are de; cient in polyunsaturated fatty acids (PUFAs) and the other was a mixed diet rich in PUFAs. Freshly metamorphosed animals from the starvation treatment had a carbon content per individual 70% lower than that of larvae fed the mixed diet. This apparent exhaustion of larval internal reserves resulted in a 50% reduction of the post-metamorphic growth rates. Growth was also reduced in animals previously fed the cyanobacterial diet. Hence, low food quantity or low food quality during the larval stage of D. polymorpha, lead to irreversible effects for post-metamorphic animals and are related to inferior competitive abilities.
Food quality effects of unsaturated fatty acids on larvae of the zebra mussel Dreissena polymorpha
(2002)
In standardized growth experiments, newly hatched larvae of the zebra mussel Dreissena polymorpha were fed diets representing different biochemical compositions. Algae that were rich in (n-3) polyunsaturated fatty acids (PUFAs), except for long-chained (.C18) PUFAs (Chlorella minutissima and Monoraphidium minutum) were of low food quality. Higher growth than on C. minutissima or M. minutum was supported by a culture of the cyanobacterium Aphanothece sp., which contained traces of a long-chained (n-3) PUFA, docosahexaenoic acid (DHA, 22 : 6n-3). The alga Isochrysis aff. galbana, which contained high amounts of the longchained (n-3) PUFAs DHA and eicosapentaenoic acid (EPA, 20 : 5n- 3), supported the highest growth. The alga Nannochloropsis limnetica, which differed from I. galbana by a defi- ciency in DHA, allowed slightly, but significantly lower, growth. Growth of larvae on N. limnetica was increased by enrichment of N. limnetica cells with a lipid extract of I. galbana, showing that larval growth on N. limnetica was limited by the deficiency of a compound that was present in I. galbana. Growth was also enhanced by feeding N. limnetica cells supplemented with DHA, but not by cells enriched with EPA, indicating that DHA was the limiting factor. We conclude that, on DHA-deficient food, the larvae of D. polymorpha were not able to sufficiently convert C18-PUFAs into long- chained (n-3) PUFAs and that the rates for elongation and desaturation of EPA into DHA limited growth.
1. Fussmann et al. (2000) presented a simple mechanistic model to explore predator-prey dynamics of a rotifer species feeding on green algae. Predictions were tested against experimental data from a chemostat system housing the planktonic rotifer Brachionus calyciflorus and the green alga Chlorella vulgaris. 2. The model accurately predicted qualitative behaviour of the system (extinction, equilibria and limit cycles), but poorly described features of population cycles such as the period and predator-prey phase relationship. These discrepancies indicate that the model lacked some biological mechanism(s) crucial to population cycles. 3. Here candidate hypotheses for the 'missing biology' are quantified as modifications to the existing model and are evaluated for consistency with the chemostat data. The hypotheses are: (1) viability of eggs produced by rotifers increases with food concentration, (2) nutritional value of algae increases with nitrogen availability, (3) algal physiological state varies with the accumulation of toxins in the chemostat and (4) algae evolve in response to predation. 4. Only Hypothesis 4 is compatible with empirical observations and thus may provide important insight into how prey evolution affects predator- prey dynamics.
A competitive immunoassay to detect a hapten using an enzyme-labelled peptide mimotope as tracer
(2002)
Mimotope peptides-peptides which mimic the binding of a hapten to its corresponding monoclonal antibody-were conjugated to peroxidase and used in competitive immunoassay. The established immunoassay was used to quantitatively determine the concentration of hapten. As model system in all the experiments described here, we used the binding of the monoclonal antibody B13-DE1 to fluorescein and the corresponding peptide mimotope.
Two Hybrid cDNA Cloning
(2002)