M.Sc. (Zoology) / Milt and blood samples of Aarbus aeneus were collected during November in order to perform chemical analyses of the blood and seminal plasma. Physical analyses were also carried out on milt. Throughout the year testes were collected in order to determine the stages of testicular development. This was done by means of histological analyses. The sperm counts averaged 8,41 x 10-3 cells rom while the spermatocrit value varied between 44% and 82% (average of 61,9%). All the milt samples collected were white in colour showing a high viscosity. Sperm motility gradually declined after activation and stopped after 82,5 seconds. Chemical values of the components tested in the blood plasma were statistically compared to those in the seminal plasma and no statistically significant differences were recorded between sodium, potassium, chloride, calcium, magnesium, glucose, total lipid, total proteien concentrations, osmolality and pH. The only component where a difference in concentration occured was fructose (30% probability). Sodium, calcium, magnesium, glucose, fructose, total lipid and total proteien concentrations in the blood plasma were significantly lower than the corresponding concentrations in the seminal plasma. In contrast the potassium concentration were higher in the seminal plasma. The pH of the seminal plasma (8,63) was alkaline while a pH of 7,5 was recorded for blood plasma. In the two lobe testis of Barbus aeneus semen is collected with seminiferous ducts into the vas deferens which together with the blood vessels are housed within a hilus. The testis is surrounded by a tunica albugenea and the seminiferous lobules are filled with cysts. The testis of the smallmouth yellowfish appears to be lobular and sperm are deposited into lumens which exist between the cysts. During the resting phase the interstitial tissue is very difficult to distinguish and is seen as a thin layer of cells between the lobules seperating them from one another...

M.Sc. (Zoology) / This investigation is divided into two sections. Section A deals with aspects of the spermatology of the tiger fish and section B deals with the cryopreservation of spermatozoa of selected freshwater fish species.

In externally fertilizing fishes, multiple factors of the spawning environment may affect the sperm viability, and thus the fertilization rate. In this thesis, the sperm activation effect of osmolality of non-electrolytes and electrolytes activation media, pH and ion channel inhibitors on Nile tilapia, Oreochromis niloticus, and the effect of environmentally relevant pollutants (cadmium, malathion and rotenone) on sperm fitness (motility and morphology) were investigated. Seminal fluid samples collected from male fishes (200-250g) were subjected to activation treatments, then analyzed for sperm motility using motility score, and motility variables using Hobson sperm tracker for straight line velocity (VSL), beat cross frequency (BCF) and percentage of motile cells (MOT). For the ion channel inhibitors and pollutants, the effect on sperm motility variables of VSL, VCL (curvilinear velocity) and LIN (linearity) were determined. Multivariate analysis was also carried out to determine the effects of ion channel inhibitors and pollutants on sperm subpopulations. The effects of pollutants on sperm morphology were observed using microscopy techniques, namely, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Sperm motility was initiated when the sperm were exposed to hypoosmotic electrolytes and non-electrolytes solution. We also found that sperm show optimal activity at pH range of 6-8 which depicts that the effect of pH on sperm motility is negligible. Lanthanum (calcium channel blocker) and flunarizine (sodium-calcium exchanger pump blocker) were found to inhibit sperm motility at 25 and 5 µM, respectively, suggesting that both ion channels play a significant role in sperm activation in O. niloticus. In contrast amiloride, ouabain and quinine showed no effects on activation, indicating that epithelial sodium channels, sodium-potassium ATPase and voltage gated potassium channels respectively are unlikely to have major roles in sperm activation or motility. The spermatozoa of Oreochromis niloticus were uniflagellate with clearly differentiated oval-shaped head, midpiece and flagellum. Sperm exposed to hypoosmotic shock showed swelling of the midpiece and sleeve structure. The pollutants showed dose- and time-dependent effect on sperm motility of the fast linear sperm subpopulation. Sperm morphology was not affected. Sperm motility was inhibited at 0.44, 0.03 and 0.063 µM, cadmium, malathion and rotenone respectively. Both cadmium and malathion exerted effects very quickly after exposure. The effect of cadmium, which can exert toxicity by calcium antagonism, is consistent with the effects of calcium channel blockes and further supports an important role for calcium in sperm activation and motility. Malathion had effects at relatively low, environmentally relevant concentrations, suggesting the presence of functionally important acetylcholinesterase activity in sperm, and also the presence of activation cytochrome P450 activity. Rotenone, a well known mitochondrial poison, affected motility only after 15 min of pretreatment. The alteration of sperm trajectories in fast linear spermatozoa subpopulation by pollutants at submicromolar concentrations as demonstrated in our study implies potentially serious consequences for fish populations in polluted environments. Furthermore the results indicate that fish sperm motility as assessed by CASA could be an ecologically relevant, sensitive, and ethically acceptable method for toxicity testing in environmental risk assessment.