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At the end of the time-out, if the sensor sees that its local area already has satisfactory coverage by other active sensors, it decides to sleep Otherwise it decides to become active and informs its neighbors about it The local area to be considered may be a small circle around the sensor that has high values for sensing Some particular sample of points from the area can be taken to reduce computation time 1149 Variations of the Sensor Area-Coverage Problem.

Figure 9-18

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At the satellite end, both clock synchronization biases, with reference to constellation time and satellite location accuracy, are certain to generate nal positioning errors. At the receiver end, clock bias and also the location of the center of phase of the antenna are sources of positioning inaccuracy. In addition, the signal does not propagate at a constant speed because of variations induced by the successive layers of the atmosphere. Additional delays can also be induced by multipath. These are physical-based potential errors, but voluntary errors were also added in the early days of GPS (Selective Availability). The main dif culties of GNSS positioning are signal acquisition and tracking, as well as error mitigation. A description of error sources is given in 6.

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RESULTS OF EXPERIMENT 2 In this experiment, the e ects of three di erent impairments packet loss, delay jitter, and network delay are measured on the combination of voice and DTMF signal transmission. Each DTMF digit is used to represent a voice clip in the Hammer script. The correlation between the DTMF and the voice clip is as presented in the legend of Figure C-4. The e ects of network impairments on voice signal transmission are measured using the PSQM score. In DTMF digit transmission, if it is recognized correctly at the other end of the channel,

In order to be able to compare the functionality of Access and InfoSphere Federation Server, we ran the same set of queries and modi cations in SQL across both systems. The following subsections outline how the two systems were prepared for the experiment and then discuss the experiment s results for both systems.

identi ed and described. Barriers between settings also delimit programs. Knowing about the setting (e.g., its purpose or intention) infers the typical behaviors of the people in that setting. Barker s conceptualization permits an understanding of environment-behavior relationships such that space might be organized in a certain way in order to meet its various purposes. Behavior settings are dynamic structures that evolve over time (Wicker, 1979, 1987). Staf ng (formerly manning) theory completes Barker s approach by proposing a set of concepts related to the number of people that the behavior setting needs in order to be functional (Barker, 1960; Wicker & Kirkmeyer, 1976). Besides key concepts like performers who carry out the primary tasks and the nonperformers who observe, the minimum number of people needed to maintain the functioning of a behavior setting is called the maintenance minimum, and the maximum is called its capacity. Applicants are people seeking to become part of the behavior setting. Overstaf ng or understaf ng is a consequence of too few or too many applicants for a behavior setting. The consequence of understaf ng is that people have to work harder and must endorse a greater range of different roles in order to maintain the functioning of the setting. They will also feel more committed to the group and endorse more important roles. On the

If f n < 0:1354, it means no neuron in this structure can cluster this input vector. So, the width should be modi ed to cover the input vector suitably or a new EBF neuron should be considered for adding into the structure. Keeping the neuron output threshold constant, the capability of membership functions for covering input vectors may be increased by enlarging the widths of membership functions. When the rst training pattern x1 ; d1 enters the network, the structure of the rst neuron is de ned as c 1 xT 1 s1 s 0 s0 s 0 T 9:14 9:15

catecholamine neurotransmitters (dopamine, epinephrine, and norepinephrine) in rats were changed in a direction counter to the age-associated changes normally seen (B S Brown et al, 1979) It is presently unclear at which age physical activity effects on neurological structure and function are the greatest Some researchers (Black, Isaacs, & Greenough, 1991) have argued that enriched movement experiences may be most beneficial for young animals to the extent that it enables them to optimize neural development, resulting in a more substantial neural reserve that can be drawn upon in old age This may explain the consistent relationship between physical activity and cognitive functioning evidenced in studies of lifelong exercise, as reported in the cross-sectional and non-intervention longitudinal studies 3.

Kaiser Meyer Olkin measure of sampling adequacy Bartlett s test of sphericity Approx. chi-square df Signi cance

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