Field studies of respiration in stream insects are few in comparison with laboratory studies. To evaluate the influence of temperature and oxygen along altitudinal gradients we measured the respiration rate of fully acclimatized larval Trichoptera, Plecoptera and Ephemeroptera under similar field conditions in streams from 400 to 3800 m above sea level in tropical Ecuador. Mean active respiration rates of the animals at 3800 m were approximately half of those at 400 m. Trichoptera showed a slightly larger difference in respiration with altitude than Ephemeroptera. Comparative respiration measurements at 100 and 50% oxygen saturation indicated that highland animals reduced their oxygen uptake more than their counterparts in the lowland when oxygen availability decreased. The temperature response of respiration calculated between the insect assemblages at different altitudes showed a mean assemblage Q 10-value of 1.50. Trichopteran larvae had a slightly stronger temperature response (Q 10 of 1.68) than ephemeropterans (Q 10 of 1.30). These community Q 10-values are considerably lower than the mean value of 2.36 found in single species in the laboratory. The weak community-wide response of respiration to temperature in tropical streams is probably due to full acclimatization of the component species to stable and narrow temperature ranges. Adaptations to the low oxygen availability at high altitude probably consist of a suite of genetic physiological and behavioural features. © Springer 2005.

Information about muscular tissue flow is important for diagnosing, treating and monitoring patients with tissue ischemia. For this purpose an objective method which is reproducible and continuous is needed. In co-operation with the company Unisense A/S, we have developed a sensor for instantaneous and continuous monitoring of muscle tissue flow in vivo. The method is based on a flexible microsensor which emits and measures minute amounts of inert tracer gases. The objective was to evaluate the capability of the microsensor to measure varying degrees of tissue flow changes and compare these measurements with the 133 Xenon Washout Technique for measuring local perfusion rates in skeletal muscle. The Unisense microsensor was tested in the gracilis muscle of six anaesthetized pigs subjected to varying degrees of muscle ischemia. We found that both tissue flow and pO2 declined in syncrony with reduced blood flow to the lower extremities. All the data from the Unisense microsensor show the same trend as the Xenon data and thus confirms that the microsensor can measure changes in tissue flow.

We determined vertical changes in current velocity and dissolved oxygen concentration in biofilms on artificial and natural substrates using microelectrodes. We used biofilms developed on glass slides dipped in an artificial stream for 3 months, artificial clay tiles dipped in an outdoor artificial stream for 3 months, and natural pebbles. In the biofilm on a glass slide, current velocity significantly decreased from the surface of the biofilm and became 0 cm s-1 at the surface of the glass slide. Vertical profile of current velocity versus depth indicated a presence of a viscous sublayer of 0.2-mm thickness above the surface of glass slide. Dissolved oxygen (DO) concentration increased within the biofilm and attained the maximum (123%) at the surface of the glass slide, indicating active photosynthesis by sessile diatoms at the layer corresponding to the observed viscous sublayer. In the biofilm on an artificial tile, DO increased to 163% saturation at 24.849-mm depth, followed by rapid decrease (6%) at the surface of the tile. A similar result of remarkable decrease in DO saturation was also found in the biofilm on a natural pebble. These results suggest that smoothness of the substrate surface is related to the vertical profile of DO saturation. The thickness of the viscous sublayer and oxygen-depleted area (up to several hundred micrometers, μm) was sufficient for the presence of bacteria, protists, and other metazoan animals, suggesting high activity and diversity of those heterotrophs in the bottom part of biofilms. © The Japanese Society of Limnology 2006.