Abstract
ABSTRACT Tools of histochemistry and digital image analysis were used to quantify changes in the coverage area of lipid droplets (lipid content) of oocytes of the penshell Atrina maura during oogenesis and to determine its relation to changes in water temperature and seston content. These data led to calculating a lipid index as a criterion of gamete development and quality. Gonads were collected monthly for 18 mo and prepared for histochcmical processing with Sudan Black B for identification of lipids. Finished slides were digitized for determining stages of oogenesis and variations in the size of oocytes. Two periods of greatest reproductive activity occurred during the study, with a lower peak from November through January (∼15°C; 26 mg/g) and a major peak from April through June (∼20°C; 25–40 mg/g). Oocyte area significantly varied during the stages of active development (516–2,743 µm2), ripeness (1,073–2,930 µm2), spawning (145–2,939 µm2), and atresia (331–2,001 µm2). Lipid incorporation into oocyte ...
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