The capacity of fading vector Gaussian channels under amplitude constraints on antenna subsets

Upper bounds on the capacity of vector Gaussian channels affected by fading are derived under peak amplitude constraints at the input. The focus is on constraint regions that can be decomposed in a Cartesian product of sub-regions. This constraint models a transmitter configuration employing a number of power amplifiers less than or equal to the total number of transmitting antennas. In general, the power amplifiers feed distinct subsets of the transmitting antennas and partition the input in independent subspaces. Two upper bounds are derived: The first one is suitable for high signal-to-noise ratio (SNR) values and, as we prove, it is tight in this regime; The second upper bound is accurate at low SNR. Furthermore, the derived upper bounds are applied to the relevant case of amplitude constraints induced by employing a distinct power amplifier for each transmitting antenna

Examination of the efficacy of acute L-alanyl-L-glutamine ingestion during hydration stress in endurance exercise

<p>Abstract</p> <p>Background</p> <p>The effect of acute L-alanyl-L-glutamine (AG; Sustamine™) ingestion on performance changes and markers of fluid regulation, immune, inflammatory, oxidative stress, and recovery was examined in response to exhaustive endurance exercise, during and in the absence of dehydration.</p> <p>Methods</p> <p>Ten physically active males (20.8 ± 0.6 y; 176.8 ± 7.2 cm; 77.4 ± 10.5 kg; 12.3 ± 4.6% body fat) volunteered to participate in this study. During the first visit (T1) subjects reported to the laboratory in a euhydrated state to provide a baseline (BL) blood draw and perform a maximal exercise test. In the four subsequent randomly ordered trials, subjects dehydrated to -2.5% of their baseline body mass. For T2, subjects achieved their goal weight and were not rehydrated. During T3 - T5, subjects reached their goal weight and then rehydrated to 1.5% of their baseline body mass by drinking either water (T3) or two different doses (T4 and T5) of the AG supplement (0.05 g·kg^-1and 0.2 g·kg^-1, respectively). Subjects then exercised at a workload that elicited 75% of their VO₂max on a cycle ergometer. During T2 - T5 blood draws occurred once goal body mass was achieved (DHY), immediately prior to the exercise stress (RHY), and immediately following the exercise protocol (IP). Resting 24 hour (24P) blood samples were also obtained. Blood samples were analyzed for glutamine, potassium, sodium, aldosterone, arginine vasopressin (AVP), C-reactive protein (CRP), interleukin-6 (IL-6), malondialdehyde (MDA), testosterone, cortisol, ACTH, growth hormone and creatine kinase. Statistical evaluation of performance, hormonal and biochemical changes was accomplished using a repeated measures analysis of variance.</p> <p>Results</p> <p>Glutamine concentrations for T5 were significantly higher at RHY and IP than T2 - T4. When examining performance changes (difference between T2 - T5 and T1), significantly greater times to exhaustion occurred during T4 (130.2 ± 340.2 sec) and T5 (157.4 ± 263.1 sec) compared to T2 (455.6 ± 245.0 sec). Plasma sodium concentrations were greater (p < 0.05) at RHY and IP for T2 than all other trials. Aldosterone concentrations at RHY and IP were significantly lower than that at BL and DHY. AVP was significantly elevated at DHY, RHY and IP compared to BL measures. No significant differences were observed between trials in CRP, IL-6, MDA, or in any of the other hormonal or biochemical measures.</p> <p>Conclusion</p> <p>Results demonstrate that AG supplementation provided a significant ergogenic benefit by increasing time to exhaustion during a mild hydration stress. This ergogenic effect was likely mediated by an enhanced fluid and electrolyte uptake.</p

The Capacity of the Amplitude-Constrained Vector Gaussian Channel

The capacity of multiple-input multiple-output additive white Gaussian noise channels is investigated under peak amplitude constraints on the norm of the input vector. New insights on the capacity-achieving input distribution are presented. Furthermore, it is provided an iterative algorithm to numerically evaluate both the information capacity and the optimal input distribution of such channel

Capacity Bounds for Amplitude-Constrained AWGN MIMO Channels with Fading

We evaluate capacity bounds for multiple-input multiple-output (MIMO) additive white Gaussian noise (AWGN) fading channels subject to input amplitude constraints. We focus on two practical cases, in which the transmitter: (i) employs a single antenna amplifier, which induces a constraint on the norm of the input vector, and (ii) it employs multiple amplifiers, one per antenna, which leads to independent constraints on the amplitude of each input vector entry. For both cases, we evaluate the asymptotic capacity gap between upper and lower bounds at high signal-to-noise ratio

A sphere packing bound for AWGN MIMO fading channels under peak amplitude constraints

An upper bound on the capacity of multiple-input multiple-output (MIMO) additive white Gaussian noise fading channels is derived under peak amplitude constraints. The tightness of the bound is investigated at high signal-to-noise ratio (SNR), for any arbitrary convex amplitude constraint region. Moreover, a numerical simulation of the bound for fading MIMO channels is analyzed, at any SNR level, for a practical transmitter configuration employing a single power amplifier for all transmitting antennas

Fatigue and Pacing in High-Intensity Intermittent Team Sport: An Update

With the advancements in player tracking technology, the topic of fatigue and pacing in team sport has become increasingly popular in recent years. Initiallybased upon a pre-conceived pacing schema, a central metabolic control system is proposed to guide the movement of players during team sport matches, which can beconsciously modified based on afferent signals from the various physiological systems and in response to environmental cues. On the basis of this theory, coupled with thecollective findings from motion-analysis research, we sought to define the different pacing strategies employed by team sport players. Whole-match players adopt a ‘slow positive’ pacing profile (gradual decline in total running intensity), which appears to be global across the different team sports. High-intensity movement also declines in a ‘slow-positive’ manner across most team sport matches. The duration of the exercise bout appears to be important for the selected exercise intensity, with the first introduction to a match as a substitute or interchange player resulting in a ‘one bout, all out’ strategy. In a limited interchange environment, a second introduction to the match results in a ‘second-bout reserve’ strategy; otherwise, the ‘one bout, all out’ strategy is likely to be adopted. These pacing profiles are proposed to reflect the presence of a central regulator that controls the movement intensity of the player to optimize performance, as well as avoiding the harmful failure of any physiological system. The presence of ‘temporary fatigue’ reflects this process, whereby exercise intensity is consciously modulated from within the framework of a global pacing schema