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THE DIMENSIONS ON A FRAME BUILDING ARE SET UP FOR THE CARPENTER, SO THE OUTSIDE OF THE FRAME IS USED AS THE DEFINITION POINT, NOT THE OUTSIDE OF THE VENEER. SINCE THE WINDOW POSITION IS KNOWN, BUT THE EXACT SIZE OF THE WINDOW IS NOT ALWAYS KNOWN UNTIL IT IS SHIPPED TO THE SITE (DUE TO CHANGES IN ORDERS, ETC.) THE WINDOWS AND DOORS ARE GENERALLY DIMENSIONED TO THE CENTER POINT.



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Timeframes for these responses range from nanoseconds (light), to milliseconds (O2, toxicity), to minutes (enzyme synthesis) or hours (sporulation) (see Section 35, Table 35, and Figure 36) This remarkable propensity of populations within naturally occurring microbial communities to change is a blessing for microbiologists practicing enrichment culture However, it is a major impediment for those seeking to interpret physiological and ecological measurements performed on laboratory-incubated environmental samples such as water, soil, or sediments The validity of measurements conducted on microbial communities removed from their original eld setting is uncertain, because we cannot be sure that conditions imposed upon the native microorganisms (postsampling and incubation) have not quantitatively or qualitatively altered their populations and physiological reactions Potentially misleading bottle effects are implicit in all measurements performed on sampled microbial communities (eg, Venrick et al, 1977; Vaulot et al, 1995).





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When cleaning printer mirrors, be sure that the power is off and that the unit is unplugged. Never ever, repeat, never look directly at the laser it could harm your eyes. Along this line, never operate the printer with its covers off. (Most printers will not power up with a cover open, anyway.)

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Therefore, for the practicing environmental microbiologist, there is considerable controversy surrounding the amount of time required for microorganisms in environmental samples to respond to sampling and experimentally induced environmental changes Implicit in many published investigations is the hypothesis that accurate qualitative and quantitative microbial activity determinations of in situ processes can be performed in the laboratory within a safe period before artifacts develop (Figure 63) This hypothesis has not been adequately tested Yet, its validity is essential for the extrapolation of results from laboratory incubations to eld sites (Staley and Konopka, 1985; Karl, 1986, 1995; Tiedje et al, 1989; Pinckney et al, 1995; Madsen, 1996, 1998a) The alternative (conservative) methodological approach views laboratory incubations of environmental samples, at best, as a means toward estimating eld processes.

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may not be viable. In such situations, we can appeal to a stochastic-gradient approximation for estimating wO. Assuming an initial training phase in which transmitted data { d ( i ) = s(z - A)} are known at the receiver (i.e., at the equalizer), we can then use the available measurements { d ( i ) ,u,}to estimate w 0 iteratively by using, e.g., the LMS recursion:

From the conservative viewpoint, quantitative extrapolation from laboratory results to actual eld processes is taboo (Karl, 1995; Madsen, 1998a) because the instant an environmental sample is removed from a.

FIGURE 19-19

We note that if the data points di are all distinct and the interpolation matrix @ is positive definite, implying that all of its elements are positive and hence is invertible, then we can solve Equation 8.46 to obtain the weight vector W, which is formulated as:

Just as the getRGB method can retrieve the values of a past setRGB method, you can transfer past setTransform values using the getTransform method.

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