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Bioassay selection

The number of environmental samples that can be tested per day, per week, or per month will depend on the bioassays selected. Available equipment in the laboratories will also dictate sample throughput capabilities. In the German Federal Institute of Hydrology, one technical assistant can process six samples per week with the test battery and protocol described herein. [Pg.135]

WASTOXHAS needs essential prerequisites for its optimal operation, namely the initial application of a large bioassay battery conducted after classical small-scale batch shaking leaching test (for example EN 12457-1 to 4, 2002 or equivalent). The final choice of bioassays selected for the battery is not self-evident, but some examples of possible bioassays are given in Table 2 and some concepts are given in Table 3 and Section 3.4. Before undertaking some bioassays, waste pre-treatment may also be required (see Section 7). [Pg.334]

General Criteria for Bioassay Selection in Allelopathy Studies.319... [Pg.328]

GENERAL CRITERIA FOR BIOASSAY SELECTION IN ALLELOPATHY STUDIES... [Pg.332]

Brassinolide was tested on 17 bioassays for growth substance. The results led to claims that brassinolide possesses a broad spectrum of biological activity, including gibberellin-, auxin- and cytokinin-like activity (32,34). These claims must be treated with some caution however, since the claimed "specificity of some of the bioassays selected is questionable. At present three bioassay techniques (35,36,37) are used routinely for the detection of brassinolide activity. All three assays are sensitive to auxin, which is a prerequisite for the detection of brassinolide-like compounds. This is not to say that brassinolide has auxin-like activity, but rather there seems to be an interaction of cooperative action between auxin and BR. [Pg.61]

Q Revise BioAssay Selection SI Select Active Add Active Add Tested... [Pg.233]

Two large studies were done (250,251) for the selection of a2o, nitro, and anthraquinone dyes for carcinogen bioassay. Based on previous information or testing, a total of 30 dyes were selected based on chemical stmcture, potential exposure, and suspicion of carcinogenicity. [Pg.387]

Scanning Electron Microscopy and X-Ray Microanalysis Principles of Electroanalytical Methods Potentiometry and Ion Selective Electrodes Polarography and Other Voltammetric Methods Radiochemical Methods Clinical Specimens Diagnostic Enzymology Quantitative Bioassay... [Pg.247]

Parasitic hymenoptera hold promise in integrated pest management schemes, because they parasitize many economically important insect pests in a species-and stage-selective manner. The pheromones and kairomones of the parasitic hymenoptera have been studied for a long time, and there are many examples where there is evidence of chemical mediation of parasitoid behavior. This review emphasizes work done since the last major reviews [11, 12, 42] and, where it is available, on the primary bioassay-guided chemical identification of the semiochemical (Fig. 2 and Tables 3 and 4). [Pg.146]

Nomura and Ogata provided the first evidence that tunicates can produce PGs [17]. Using a rat stomach fundus bioassay, Halocynthia roretzi tissues were shown to possess low levels of PGs. The testes showed higher levels (9 ngg-1 wet tissue) than ovary and muscle tissue. The sea-squirt Styela clava did not show PGs by this method. No structures were determined in this work. Reexamination of the ability of H, roretzi to produce PGs was carried out by Ogata and coworkers [19]. Incubation of selected tissues with 14C-labeled eicosa-8,11,14-trienoic acid and subsequent isolation of PGE and PGF fractions after addition of carrier showed the branchial tissue to have the highest conversion levels. Quantitation was done by LSC. Using a TLC radioscanner, the authors determined that fractions with metabolites similar to PGE and PGF... [Pg.176]

The main advantage of this technique is the rapidity of response and the possibility of performing many bioassays with different algal strains at the same time. The disadvantage is that the kind of response is qualitative. This limitation can be overcome by selecting for liquid inhibition bioassays, the strains that give a positive response in paper disk bioassay (i.e. the strains sensitive to the allechemical(s) tested). [Pg.49]

A prerequisite to pharmacokinetic/pharmacodynamic studies is the availability of a sufficiently selective and sensitive assay. The assay must be capable of detecting and accurately quantifying the therapeutic protein in the presence of a complex soup of contaminant molecules characteristic of tissue extracts/body fluids. As described in Chapter 7, specific proteins are usually detected and quantified either via immunoassay or bioassay. Additional analytical approaches occasionally used include liquid chromatography (e.g. HPLC) or the use of radioactively labelled protein. [Pg.75]

Most commonly, bioassays for the evaluation of the acute toxic effects of pesticides are based on single aquatic species selected to be representative of a range of taxonomic and functional groups, i.e., bacteria, algae, invertebrates or fish [ 53,54]. Generally, toxicity evaluation using a single species is the alternative of choice rather than the use of multiple species, because extrapolation of effects to an ecosystem is more difficult and can often lead to incorrect conclusions. [Pg.66]

The selection of suitable single species and protocols is not a trivial task and may be dependent on various factors. Some of these include simplicity, low cost, or modest material and equipment demand. However, a higher sensitivity than other species to toxicants may be decisive in this choice in order to serve as warning systems. Table 1 shows the sensitivity in terms of effective concentration (EC50), which is the toxicity endpoint for the organisms (bacteria, crustaceans, algae, and fish) selected for the toxicity bioassays. These toxicity bioassays are usually classified according to the test species involved. [Pg.66]

The ideal species for carcinogenicity bioassays should absorb, metabolize, and excrete the compound under study exactly as humans do. Unfortunately, because of the small number of species that meet the other criteria for selection, there is limited practical utility to this important scientific concept, as applied to carcinogenicity studies. [Pg.302]


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Functional bioassays selection

Selection criteria for bioassays

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