{"title":"Effects of dilution rates, animal species and instruments on the spectrophotometric determination of sperm counts.","authors":"M Rondeau, M Rouleau","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Using semen from bull, boar and stallion as well as different spectrophotometers, we established the calibration curves relating the optical density of a sperm sample to the sperm count obtained on the hemacytometer. The results show that, for a given spectrophotometer, the calibration curve is not characteristic of the animal species we studied. The differences in size of the spermatozoa are probably too small to account for the anticipated specificity of the calibration curve. Furthermore, the fact that different dilution rates must be used, because of the vastly different concentrations of spermatozoa which is characteristic of those species, has no effect on the calibration curves since the dilution rate is shown to be artefactual. On the other hand, for a given semen, the calibration curve varies depending upon the spectrophotometry used. However, if two instruments have the same characteristic in terms of spectral bandwidth, the calibration curves are not statistically different.</p>","PeriodicalId":21345,"journal":{"name":"Revue canadienne de biologie","volume":"40 2","pages":"173-80"},"PeriodicalIF":0.0000,"publicationDate":"1981-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revue canadienne de biologie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Using semen from bull, boar and stallion as well as different spectrophotometers, we established the calibration curves relating the optical density of a sperm sample to the sperm count obtained on the hemacytometer. The results show that, for a given spectrophotometer, the calibration curve is not characteristic of the animal species we studied. The differences in size of the spermatozoa are probably too small to account for the anticipated specificity of the calibration curve. Furthermore, the fact that different dilution rates must be used, because of the vastly different concentrations of spermatozoa which is characteristic of those species, has no effect on the calibration curves since the dilution rate is shown to be artefactual. On the other hand, for a given semen, the calibration curve varies depending upon the spectrophotometry used. However, if two instruments have the same characteristic in terms of spectral bandwidth, the calibration curves are not statistically different.