Oxygen uptake, heart rate and activities of locomotor muscles during a critical swimming speed protocol in the gilthead sea bream Sparus aurata.

Oxygen uptake, heart rate and contraction frequencies of slow oxidative (SO) and fast glycolytic (FG) muscle were measured simultaneously in gilthead seabream Sparus aurata submitted to stepwise increases in current speed in a swimming respirometer. Variation in oxygen uptake was closely related to variation in heart rate, over initial steps these rose in concert with an increase in contraction frequency of SO muscle. There was an asymptote in oxygen uptake and heart rate at high speeds that reflected a transition from exclusive use of aerobic SO muscle to a combination of SO and anaerobic FG muscle, and which preceded fatigue.

Very Low Resource Digital Implementation of Bioimpedance Analysis.

Bioimpedance spectroscopy consists of measuring the complex impedance of biological tissues over a large frequency domain. This method is particularly convenient for physiological studies or health monitoring systems. For a wide range of applications, devices need to be portable, wearable or even implantable. Next generation of bioimpedance sensing systems thus require to be implemented with power and resource savings in mind. Impedance measurement methods are divided into two main categories. Some are based on "single-tone" signals while the others use "multi-tone" signals. The firsts benefit from a very simple analysis that may consist of synchronous demodulation. However, due to necessary frequency sweep, the total measurement may take a long time. On the other hand, generating a multi-frequency signal allows the seconds to cover the whole frequency range simultaneously. This is at the cost of a more complex analysis algorithm. This makes both approaches hardly suitable for embedded applications. In this paper, we propose an intermediate approach that combines the speed of multi-tone systems with a low-resource analysis algorithm. This results in a minimal implementation using only adders and synchronous adc. For optimal performances, this small footprint digital processing can be synthesized and embedded on a mixed-mode integrated circuit together with the analog front-end. Moreover, the proposed implementation is easily scalable to fit an arbitrary frequency range. We also show that the resulting impact on noise sensitivity can be mitigated.

Effects of extraction method and storage of dry tissue on marine lipids and fatty acids.

Various protocols are currently used to study marine lipids, but there is a growing interest in working on dry samples that are easier to transport. However, reference protocols are still lacking for dry samples. In order to make recommendations on this use, lipid classes and fatty acids (FA) obtained from six analytical protocols using two different tissue states (dry vs wet) and three extraction methods (automat vs manual potter vs leaving the solvent to work on tissue) were compared. Three dry storage modes of tissue (freezer vs gas nitrogen vs dry room) during one and three months were also compared. These comparisons were made on seven marine species with different lipid profiles, including fishes, crustaceans and mollusks. Lipid classes and FA obtained from wet and dry tissues were similar, but they were affected by the extraction methods. Regardless of tissue state, "Leave to work" methods obtained the highest lipid quantities, followed by manual potter and automat methods (ca. 90% and 80% of "Leave to work" methods, respectively). Linear relationships allowed correction for lipid classes and FA concentrations obtained from different protocols. The repeatability of all protocols still needs to be improved, especially for fish species. Increasing the replicate number for each sample might be an indirect way to improve lipid quantification. Our results show that storing dry tissues in the freezer for more than one month was associated with a decrease in lipids, which is also observed for other storage methods. For qualitative studies of FA (expressed in %), a three-month storage of dry tissue in freezer did not affect the relative composition of species/tissues with a lipid content below 20% of dry weight.