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  • 1.1. The effects of thermal acclimatization at 10 and 24°C on heart rate were investigated on unrestrained soles (Solea vulgaris).
  • 2.2. The sensitivity of heart rate to temperature changes induced by temperature acclimatization was higher in cold-acclimatized than in warm-acclimatized soles.
  • 3.3. Heart rate of cold-acclimatized fish to temperature changes was not affected by blocking the vagal tone with atropine.
  • 4.4. After atropine treatment the ability of heart rate to show thermal compensation decreased in warm-acclimatized soles.
  • 5.5. It is suggested that the vagus nerve can function differently at different temperatures.
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A site in the western part of Long Island Sound was monitored from January 2000 to May 2002. The littoral was divided into five different zones from the supra-littoral fringe (A) to the infra-littoral fringe (E). The midshore was dominated by Fucus vesiculosus L. and the sublittoral fringe by Chondrus crispus Stackh. There was a significant change in community structure over the years and the predominant change occurred between 2001 and 2002. The alternation in community structure was caused by an increase in abundance of species like Porphyra suborbiculata Kjellm., Porphyra leucosticta Type A and C (Neefus et al. 2000), Ceramium virgatum Roth, and Codium fragile subsp. tomentosoides (van Goor)Silva and a decrease in abundance in Fucus vesiculosus, Blidingia minima (Nägeli ex Kütz.) Kylin and Ulva lactuca L. The changes in community structure coincided with the change in environmental conditions. Air temperature as well as surface seawater temperature (depth <2 m) were the most important factors of those analyzed. Temperature seems to be the bottom-up force regulating the community structure.  相似文献   

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Background

Exposure to future ocean acidification scenarios may alter the behaviour of marine teleosts through interference with neuroreceptor functioning. So far, most studies investigated effects of ocean acidification on the behaviour of fish, either isolated or in combination with environmental temperature. However, only few physiological studies on this issue were conducted despite the putative neurophysiological origin of the CO2-induced behavioural changes. Here, we present the metabolic consequences of long-term exposure to projected ocean acidification (396–548 μatm PCO2 under control and 915–1272 μatm under treatment conditions) and parallel warming in the brain of two related fish species, polar cod (Boreogadus saida, exposed to 0 °C, 3 °C, 6 °C and 8 °C) and Atlantic cod (Gadus morhua, exposed to 3 °C, 8 °C, 12 °C and 16 °C). It has been shown that B. saida is behaviourally vulnerable to future ocean acidification scenarios, while G. morhua demonstrates behavioural resilience.

Results

We found that temperature alters brain osmolyte, amino acid, choline and neurotransmitter concentrations in both species indicating thermal responses particularly in osmoregulation and membrane structure. In B. saida, changes in amino acid and osmolyte metabolism at the highest temperature tested were also affected by CO2, possibly emphasizing energetic limitations. We did not observe changes in neurotransmitters, energy metabolites, membrane components or osmolytes that might serve as a compensatory mechanism against CO2 induced behavioural impairments. In contrast to B. saida, such temperature limitation was not detected in G. morhua; however, at 8 °C, CO2 induced an increase in the levels of metabolites of the glutamate/GABA-glutamine cycle potentially indicating greater GABAergic activity in G.morhua. Further, increased availability of energy-rich substrates was detected under these conditions.

Conclusions

Our results indicate a change of GABAergic metabolism in the nervous system of Gadus morhua close to the optimum of the temperature range. Since a former study showed that juvenile G. morhua might be slightly more behaviourally resilient to CO2 at this respective temperature, we conclude that the observed change of GABAergic metabolism could be involved in counteracting OA induced behavioural changes. This may serve as a fitness advantage of this respective species compared to B. saida in a future warmer, more acidified polar ocean.
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A new strain of Chlorella sp. (Chlorella-Arc), isolated from Arctic glacier melt water, was found to have high specific growth rates (μ) between 3 and 27 °C, with a maximum specific growth rate of 0.85 day?1 at 15 °C, indicating that this strain was a eurythermal strain with a broad temperature tolerance range. To understand its acclimation strategies to low and high temperatures, the physiological and biochemical responses of the Chlorella-Arc to temperature were studied and compared with those of a temperate Chlorella pyrenoidosa strain (Chlorella-Temp). As indicated by declining F v/F m, photoinhibition occurred in Chlorella-Arc at low temperature. However, Chlorella-Arc reduced the size of the light-harvesting complex (LHC) to alleviate photoinhibition, as indicated by an increasing Chl a/b ratio with decreasing temperatures. Interestingly, Chlorella-Arc tended to secrete soluble sugar into the culture medium with increasing temperature, while its intracellular soluble sugar content did not vary with temperature changes, indicating that the algal cells might suffer from osmotic stress at high temperature, which could be adjusted by excretion of soluble sugar. Chlorella-Arc accumulated protein and lipids under lower temperatures (<15 °C), and its metabolism switched to synthesis of soluble sugar as temperatures rose. This reflects a flexible ability of Chlorella-Arc to regulate carbon and energy distribution when exposed to wide temperature shifts. More saturated fatty acids (SFA) in Chlorella-Arc than Chlorella-Temp also might serve as the energy source for growth in the cold and contribute to its cold tolerance.  相似文献   

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  • 1.1.|Air temperature within the external auditory meatus, sensed by a thermistor insulated from the walls of the aural canal, was compared with the temperature recorded from a probe in the esophagus in patients under general anaesthesia.
  • 2.2.|In the first study of 14 patients, aural temperatures at the time of induction of anaesthesia were more than 3°C lower, and the changes during surgery were more variable, than those recorded from the esophagus.
  • 3.3.|In a second study of 35 patients in which heat loss from the external ear was reduced by ear protectors, there was also a poor correlation between temperatures of the ear and esophagus. Aural temperature was initially lower and rose over time in most cases whereas esophageal temperature generally decreased.
  • 4.4.|These results suggest that air temperature within the aural canal is not a useful estimate of deep body temperature since it reflects mainly skin temperature.
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