The purpose was to determine the aerobic power (maximal oxygen uptake) and body composition of older track athletes after a 20-yr follow-up (T3). At 20 yr, 21 subjects [mean ages: 50.5 +/- 8.5 yr at initial evaluation (T1), 60.2 +/- 8.8 yr at 10-yr follow-up (T2), and 70.4 +/- 8.8 yr at 20-yr follow-up (T3)] were divided into three intensity groups: high (H; remained elite; n = 9); moderate (M; continued frequent moderate-to-rigorous endurance training; n = 10); and low (L; greatly reduced training; n = 2). All groups decreased in maximal oxygen uptake at each testing point (H, 8 and 15%; M, 13 and 14%; and L, 18 and 34% from T1 to T2 and T2 to T3, respectively). Maximal heart rate showed a linear decrease of approximately 5-7 beats.min-1.decade-1 and was independent of training status. Body weight remained stable for the H and M groups and percent fat increased approximately 2-2.5%/decade. Although fat-free weight decreased at each testing point, there was a trend for those who began weight-training exercise to better maintain it. Cross-sectional analysis at T3 showed that leg strength and bone mineral density were generally maintained from age 60 to 89 yr. Those who performed weight training had a greater arm region bone mineral density than those who did not. These longitudinal data show that the physiological capacities of older athletes are reduced despite continued vigorous endurance exercise over a 20-yr period (approximately 8-15%/decade). Changes in body composition appeared to be less than those shown for the healthy sedentary population and were related to changes in training habits.
Twelve healthy, male Army recruits performed three, 40-min treadmill marches at 6 km/h, under three load carriage conditions: 0%-body weight (BW) backpack load, 15%-BW load and 30%-BW load. Kinematic and kinetic data were obtained, immediately before and after each treadmill march, for computing ankle, knee and hip joint rotations and moments. Metabolic data (oxygen uptake (VO2), expired ventilation (VE), respiratory exchange ratio (RER)), heart rate (HR) and ratings of perceived exertion (RPE) were collected continuously during marching. Significant differences (p < or = 0.05) were observed between each load for VO2, HR and VE throughout the marches. At 40 min, relative energy costs for 0%-BW, 15%-BW and 30%-BW loads were 30, 36 and 41% VO2max, respectively. RPE responses during marching significantly differed for only the 30%-BW load and were greater than responses at 0%-BW and 15%-BW loads. During load carriage trials prior to treadmill marches (pre-march), peaks in internal, hip extension, knee extension and ankle plantar flexion moments increased with increasing backpack load. Relative to 0%-BW load, percentage increases in knee moments, due to 15%-BW and 30%-BW loads, pre-march, were substantially larger than the percentage increases for hip extension and plantar flexion moments, pre-march. Pre-march and post-march peaks in hip extension and ankle plantar flexion moments were similar with all loads, while notable pre-march to post-march declines were observed for knee extension moment peaks, at 15%-BW and 30%-BW load. Pre-march joint loading data suggests that the knee may be effecting substantial compensations during backpack loaded marching, perhaps to attenuate shock or reduce load elsewhere. Post-march kinetic data (particularly at 15%-BW and 30%-BW load), however, indicates that such knee mechanics were not sustained and suggests that excessive knee extensor fatigue may occur prior to march end, even though overall metabolic responses, at 15%-BW and 30%-BW load, remained within generally recommended limits to prevent fatigue during prolonged work.
Analyses of extracts of pheromone glands and of volatiles from calling female fall armyworm moths,Spodoptera frugiperda (J.E. Smith), revealed the presence of the following compounds: dodecan-1-ol acetate, (Z)-7-dodecen-1-ol acetate, 11-dodecen-1-ol acetate, (Z)-9-tetradecenal, (Z)-9-tetradecen-1-ol acetate, (Z)-11-hexadecenal, and (Z)-11-hexadecen-1-ol acetate. The volatiles emitted by calling females differed from the gland extract in that the two aldehydes were absent. Field tests were conducted with sticky traps baited with rubber septa formulated to release blends with the same component ratios as those emitted by calling females. These tests demonstrated that both (Z)-7-dodecen-1-ol acetate and (Z)-9-tetradecen-1-ol acetate are required for optimum activity and that this blend is a significantly better lure than either virgin females or 25 mg of (Z)-9-dodecen-1-ol acetate in a polyethylene vial, the previously used standard. Addition of the other three acetates found in the volatiles did not significantly increase the effectiveness of the two-component blend as a bait for Pherocon 1C or International Pheromones moth traps.
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