Diving vertebrates are constrained by an aquatic existence because they carry a limited store of oxygen whilst submerged and must return to the surface to breathe. Therefore, oxygen stores must be used efficiently in order to maximise aerobic dive duration. The ability to use additional, non-pulmonary gas exchange to obtain oxygen from the water provides a mechanism to alleviate the use of body oxygen stores and extend dive duration. The partitioning of gas exchange between aerial and aquatic modes is predicted by the theory of optimal breathing. As the cost of obtaining oxygen by one mode increases, the reliance on this mode should decrease whilst the reliance on the alternate mode should increase. A number of environmental, physiological and ecological factors can affect metabolic rate and/or the partitioning of gas exchange between aerial and aquatic modes, with consequences for dive duration. The overall aim of this study was to examine the effects of temperature, specific dynamic action and predation on respiratory partitioning and diving behaviour in the Arafura filesnake, Acrochordus arafurae. Filesnakes provide an excellent model to address the aims of this study because they are fully-aquatic and respire bimodally, utilising both aerial and aquatic (cutaneous) gas exchange. Metabolic rate and diving behaviour are usually thermally dependent in diving ectotherms. Given this knowledge, we tested whether A. arafurae was capable of up-regulating cutaneous oxygen uptake to compensate for the temperature induced increases in metabolic rate. Metabolic rate had a Q10(20-32°C) of 2.33, however cutaneous oxygen uptake was independent of temperature and all elevated metabolic demands were met by increasing aerial oxygen uptake. Consequently, maximum dive duration was reduced by 70%, from 77 min at 20°C to 28 min at 32°C. The temperature independence of cutaneous oxygen uptake suggests that blood PO2 remained stable across temperatures and the increased blood flow expected with an elevated metabolic rate did not enhance the capacity for oxygen uptake (diffusion limited rather than perfusion limited). Although cutaneous oxygen uptake was not regulated, its contribution to extending dive duration was significant. When the ability to respire aquatically was removed (severe hypoxia), dive duration was reduced by up to 30%. Acrochordus arafurae feeds infrequently on large, high-protein meals thus the postprandial metabolic response was significant. Meal size and fast length (13 days or one month) were both positively related to the peak metabolic scope. After fasting for one month, peak rate of oxygen consumption was up to 12-fold standard metabolic rate (SMR) with the largest meal size. By comparison, an animal that was fasted for 13 days and fed an equivalent meal size incurred a six-fold increase in SMR. The energetic costs of digestion (specific dynamic action, SDA) increased with meal size, but fast length had no effect, suggesting the up-regulation of gut function was not a significant cost in the SDA. Pulmonary and cutaneous gas exchange increased with elevated metabolic demands however pulmonary oxygen uptake was the dominant mode. Despite the increase in cutaneous oxygen uptake during digestion, maximum dive duration decreased by between 50% and 90% of fasted values. The significant reductions in dive duration following feeding may have implications for predator vulnerability. Diving animals are most vulnerable to predation at the water’s surface. The theory of optimal diving under predation predicts that animals should make shorter, more frequent surface intervals or longer, less frequent surfacing intervals to minimise exposure to predators. Acrochordus arafurae is prone to aerial (birds of prey) and aquatic (crocodiles, large fish) predation. Simulated avian predation did not change dive or surface duration or proportion of time at the surface or spent active. However, a greater number of longer dives were observed with fewer long surface intervals suggesting an increase in the use of cutaneous oxygen uptake. The nocturnal diving patterns of A. arafurae provide an in-built anti-predator strategy. The threat of aquatic predation by a large fish produced atypical anti-predator responses; A. arafurae became increasingly active, reduced dive duration and increased surface interval which was indicative of a foraging response. The field diving behaviour of adult A. arafurae was determined using acoustic telemetry and interpreted in the context of environmental and ecological conditions. The mean dive duration was 6.6 min, with 85% of dives less than 10 min in duration. The maximum dive duration was 153 min. There was no diel pattern in dive duration. Snakes were located at an mean depth of 0.62 m, however, they occasionally ventured to greater depths (up to 6 m) but very infrequently. Snake body temperature reflected water temperature and fluctuated by approximately 1°C on a daily basis. The short and shallow dives of A. arafurae minimise travel costs associated with surfacing and may be an anti-predator strategy. Metabolic rate and respiratory partitioning is dependent on physiological and ecological factors with consequences for dive duration. Temperature and postprandial induced increases in metabolic demands were met by increasing the reliance on aerial gas exchange given the limitations of cutaneous gas exchange; and dive duration was substantially reduced as a result. Ecological factors, such as predation, can increase the cost of surfacing and promote the use of aquatic gas exchange. However, changes to behaviour, including habitat choice, residence depth and the employment of a diving strategy that does not maximise dive duration may be just as effective at minimising the costs and maximising the gains of a dive.

Title: Comparison of universal and specific functional stress tests of ski-mountaineerers. Objectives: The aim of the thesis is to compare maximal functional parameters of ski-mountaineerers measured during three functional laboratory stress tests. The functional stress tests were set on a treadmill, bicycle ergometer, and on a ski-mountaineer trainer. Consecutively, there is evaluated the meaning of testing of the functional parameters on the ski-mountaineer trainer. Methods: Interindividual and intraindividual descriptive study of 10 ski-mountaineerers of middle and high level performance. Results: The respondents reached the average value of VO2max 63,3 ml.kg-1 .min-1 on the ski-mountaineer trainer, 67,5 ml.kg-1 .min-1 on a treadmill and 66,5 ml.kg-1 .min-1 on a bicycle ergometer. The average measured HR on the ski-mountaineer trainer was 179 heartbeats/min, on the treadmill 185 heartbeats/min and on the bycicle ergometer 183 heartbeats/min. The average value of R reached the value of 1,09 on the ski-mountaineer trainer, 1,18 on the treadmill and 1, 19 on the bycicle ergometer. The highest measured value of VO2max reached on the treadmill was 79,3 ml.kg-1 .min-1 , the bycicle ergometer enabled to reach maximum 76,5 ml.kg-1 .min-1 and the highest value reached on the ski-mountaineer trainer was...

Title: Functional Profile of Performance Billiard Players Objectives: The main aim of thesis was to find out maximal functional characteristics and body composition of performance billiard players by using laboratory testing. Next step was to define load intensity during simulated match. Methods: There were used biomedical measurements as a body measuring, bioelectrical impedance, laboratory spiroergometric measuring by maximal stress testing. Field spiroergometric measuring was provide during simulated match in pool hall. To find the role of physical fitness in performance billiard were used half structured interview with open questions and online survey. Results: The findings show that tested billiard players achieve levels of physical fitness from average to very good values. But some of them are classified as overweight and obese. Long-time playing billiard does not have any important influence on asymetric composition of muscle mass of upper limbs. During playing billiard an oxygen consumption didn't get over 30% of VO2max and values of heart rate were between 39 to 59% HRmax. During playing billiard an energy expenditure grows from 222 to 330% of BM. Billiard energetic demands of tested players are moving between 14,6 kJ to 29,3 kJ. Another result of thesis is a statement about the role of...