Unequivocal effect

Thyroxine is one of the few hormones for which unequivocal effects on isolated biochemical systems can be observed in particular, it has been shown that thyroxine at high concentrations has a direct effect on mitochondrial oxidation. Tissues from animals which have been injected with thyroid extracts or purified thyroxine show a raised oxygen consumption, particularly in liver and muscle. Similarly the addition of thyroxine to tissue slices of the same organs results in increased oxidation. Thyroxine seems to be especially trapped by the mitochondria, where it stimulates the... 

The LOEC (lowest observed effect concentration), or threshold level of observed effects, is the lowest test concentration at which a substance is observed to have a statistically significant and unequivocal effect on the test species. The NOEC (no observed effect concentration) is the highest tested concentration below the LOEC where the stated effect was not observed. A chronic toxicity test may include more than one generation of the test organism. 

This study was therefore the first one to show unequivocal effects of CLA on body composition and body weight with gold standard measmements. Most importantly, these results were not related to changes in diet or exercise habits. To our knowledge there have been no other long-term studies with CIA supplementation published yet. 

The molecular weight of lignin in the wood, ie, of protolignin, is unknown. In addition to difficulties of isolation and purification, the polymer exhibits strong solvent, ionic, and associative effects in solution. An unequivocal method of measurement has not been developed. The polymer properties of lignin and its derivatives have been discussed (10,16). 

This solution gives unequivocally the effective control range of both unflanged and flanged openings when the exhaust flow rate and velocity of the idealized cross-draft are known. The distance from the hood opening to the dividing streamline for a hood in uniform flow perpendicular to its axis is thus... 

Unequivocal syntheses of cis- and mns-(i -decahydroquinoxalincs have been achieved by lithium aluminum hydride reduction of the corresponding cis- and trans-decahydroquinoxaIin-2-ones. The latter compounds were prepared by condensation of chloroacetic acid and cis- and trans-1,2-diaminocyclohexane, respectively. The resolution of frans-dUdecahydroquinoxaline was effected by use of first dibenzoyl-cZ-tartaric acid and then of dibenzoyl- -tartaric acid. "" (C/. p. 215.)... 

We mention Williams work briefly here because it may also explain Blangey s observations strongly basic primary amines unequivocally form 7V-nitrosoanilinium ions in strongly acidic media. In contrast to the rate-limiting deprotonations of the less basic aromatic and heteroaromatic nitrosoamine cations discussed in this section, the TV-nitroso cation of a strongly basic amine deprotonates extremely slowly. Therefore, the nitroso rearrangement, the Fischer-Hepp reaction, competes effectively with the 7V-deprotonation. 

The first unequivocal evidence for the AE + DE mechanism came in three papers by Zollinger (1955 a-c) dealing with general base catalysis and primary kinetic hydrogen isotope effects in azo coupling reactions of various types. Three classes of reactions were identified i) reactions with no isotope effects (ArH/A D - 1.0) and no general base catalysis, ii) others with large isotope effects (k /k — 6.5) and (practically) linear base catalysis, and iii) intermediate cases with isotope effects of around 3.0 and less-than-linear base catalysis. 

The existence or nonexistence of conjugative effects involving the sulfone group in thiophene dioxides (a problem analogous to that in thiirene oxide and dioxide systems2,1 ) has been the subject of many studies resulting, nonetheless, in no unequivocal conclusion280. 

A major complication in applying radiation chemical techniques to ion-molecule reaction studies is the formation of nonionic initial species by high energy radiation. Another difficulty arises from the neutralization of ions, which may also result in the formation of free radicals and stable products. The chemical effects arising from the formation of ions and their reactions with molecules are therefore superimposed on those of the neutral species resulting from excitation and neutralization. To derive information of ion-molecule reactions, it is necessary to identify unequivocally products typical of such reactions. Progress beyond a speculative rationalization of results is possible only when concrete evidence that ionic species participate in the mechanism of product formation can be presented. This evidence is the first subject of this discussion. 

The copper system appears to behave similarly to the silver system, and it may be used here in order to illustrate the idea of "selective, naked-cluster cryophotochemistry 150,151). A typical series of optical-spectral traces that illustrate these effects for Cu atoms is given in Fig. 15, which shows the absorptions of isolated Cu atoms in the presence of small proportions of Cu2, and traces of Cus molecules. Under these concentration conditions, the outcome of 300-nm, narrow-band photoexcitation of atomic Cu is photoaggregation up to the Cus stage. The growth-decay behavior of the various cluster-absorptions allows unequivocal pinpointing of UV-visible, electronic transitions associated with Cuj and Cus 150). With the distribution of Cui,2,3 shown in Fig. 15, 370-nm, narrow-band excitation of Cu2 can be considered. Immediately apparent from these optical spectra is the growth (—10%) of the Cu atomic-resonance lines. Noticeable also is the concomitant... 

In many analyses, fhe compound(s) of inferesf are found as par of a complex mixfure and fhe role of fhe chromatographic technique is to provide separation of fhe components of that mixture to allow their identification or quantitative determination. From a qualitative perspective, the main limitation of chromatography in isolation is its inability to provide an unequivocal identification of the components of a mixture even if they can be completely separated from each other. Identification is based on the comparison of the retention characteristics, simplistically the retention time, of an unknown with those of reference materials determined under identical experimental conditions. There are, however, so many compounds in existence that even if the retention characteristics of an unknown and a reference material are, within the limits of experimental error, identical, the analyst cannot say with absolute certainty that the two compounds are the same. Despite a range of chromatographic conditions being available to the analyst, it is not always possible to effect complete separation of all of the components of a mixture and this may prevent the precise and accurate quantitative determination of the analyte(s) of interest. 

Qualitative (identification) applications depend upon the comparison of the retention characteristics of the unknown with those of reference materials. In the case of gas chromatography, this characteristic is known as the retention index and, although collections of data on popular stationary phases exist, it is unlikely that any compound has a unique retention index and unequivocal identification can be effected. In liquid chromatography, the situation is more complex because there is a much larger number of combinations of stationary and mobile phases in use, and large collections of retention characteristics on any single system do not exist. In addition, HPLC is a less efficient separation... 

The examples chosen above have illustrated how CVF or MS-MS may be used to generate useful structural information but these do not always provide sufficient detail to allow an unequivocal structural assigmnent. There may still be instances where it might be necessary to probe fragmentation pathways further. This can be accomplished by combining MS-MS with CVF, i.e. use CVF to effect fragmentation of an ion of interest and then study one of the product ions so formed by using conventional MS-MS. This may be considered to be MS-MS-MS . 

The discussion above lacks basic data the purpose of our inventory is mainly to raise issues that need to be addressed in the future, and to try to develop a framework that relates these issues to each other, than to supply this lacking data. Because of that, the question of whether aspects of isotopic variation discussed above can be unequivocally identified in the archaeological record in Europe cannot yet be answered. We can, however, state that some form of patterning (as opposed to random variation) can often be observed. In many cases we observe patterns without knowing the precise causes, conceivably because they are the result of more than one factor e g., a climatic and a cultural effect. 

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