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chapter 3 - RiuNet

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GENERAL INTRODUCTION<br />

in fish (Kime et al., 2001; Fauvel et al., 2010; Boryspholets et al., 2013).<br />

However, the most used technique to assess sperm motion has been<br />

subjective evaluation, and some problems have emerged from this method.<br />

In this respect, the subjective assessment depends on an experienced<br />

observer, and several aspects such as sperm density, sperm velocity, drift,<br />

etc. can cause over- or underestimation readings. Therefore, the low<br />

reproducibility of this motility analysis through subjective evaluation, which<br />

can result in variations of 30 to 60% from the same sample, often makes it<br />

difficult to interpret and compare the results between labs (Verstegen et<br />

al., 2002; Rosenthal et al., 2010). In this sense, the gradual appearance of<br />

computerized techniques has provided us with an objective and rapid<br />

method for obtaining a correct and accurate evaluation of sperm motion<br />

features (Rurangwa et al., 2004, Cabrita et al., 2011).<br />

3.2 New tools to determine sperm quality<br />

The appearance of Computer Assisted Sperm Analysis (CASA) systems has<br />

made it possible to estimate a higher number of sperm motion parameters<br />

using an objective, sensitive and accurate technique. These systems are the<br />

evolution of multiple photomicrography exposure and video-micrography<br />

techniques for spermatozoa track, using a computer equipped with imaging<br />

software (Rurangwa et al., 2004). This technique was first introduced in the<br />

80´s in mammalian sperm and only in the last few years have modern CASA<br />

systems been adapted for fish spermatozoa studies (Van Look et al., 2000;<br />

Wilson-Leedy and Ingermann, 2007). The differences in the biology of fish<br />

and mammalian spermatozoa may explain the delay in the release of<br />

adequate tools for the measurement of sperm motility in fish. To date,<br />

these systems have been used and validated in a wide range of animal<br />

groups such as marine invertebrates (Gallego et al., 2013), birds (Kleven et<br />

al., 2009), marine mammals (Montano et al., 2012), reptiles (Tourmente et<br />

al., 2011) or even insects (Al-lawati et al., 2009).<br />

A long time ago and by subjective assessment, the experimented observer<br />

was only able to estimate two sperm motion traits: the percentage of<br />

motile sperm cells and the total duration of spermatozoa movement. Then,<br />

18

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