Changes in reproductive condition in the New Zealand snapper Pagrus aurnfus (Bloch & Schneider) were monitored in a wild population over three successive years. Recrudescence occurred in spring with spawning beginning in October and continuing for 3 to 5 months. The initiation ofspawning varied by up to 3 weeks and was associated with sea surface temperatures of 15-16" C. Theconclusion ofspawning wasassociated with temperatures of 19-21" C but showed greater interannual variation than the onset of spawning. Changes in the gonadosomatic index were accompanied by parallel changes in hepatosomatic index in females but not males, reflecting the role of the liver in vitellogenesis in females.
SynopsisNew Zealand snapper, Pagrus auratus, were captured by trawling from NE New Zealand over two successive spawning seasons, and examined for acute temporal changes in gonad condition. Fish with oocytes completing final oocyte maturation predominated during the morning, with a peak in ovulated fish occurring just after midday. Afternoon catches were dominated by fish in which the most advanced oocytes had yet to begin final maturation. This suggests that ovulation is synchronised to occur soon after midday, and the high proportion (up to 100% of the catch) of fish with particular gonad stages captured at any one time indicates that daily spawning involves most of the population. Diurnal changes in oocyte diameter support a daily spawning rhythm, with numbers of large hydrated oocytes peaking in the late morning, followed by the disappearance of these oocyte stages in the afternoon. Snapper captured alive by longlining were returned to the laboratory to examine the relationship between ovulation and probable time of spawning. Unovulated fish generally ovulated close to midday on the day of capture (morning captures), or the following day (afternoon captures). The viability of ovulated eggs (proportion undergoing division after fertilization) decreased markedly after oviduct residence times of over 8 hours. This suggests that natural spawning occurs before the late evening. The results of this study are consistent with anecdotal evidence suggesting that spawning occurs every day during the late afternoon or early evening, and is similar to the reproductive patterns displayed by a number of closely related sparids.
Success, progression and retention of students are goals of many university strategic directions and policies. For many decades it has been recognised that the greatest focus in any retention strategy should be on first-year students. University of Otago too has goals around student success. The Strategic Plan of the institution also identified that in the context of a fiscally constrained environment, all of our activities and processes need to be assessed for efficiency and effectiveness. To this end, a pilot was undertaken in one area of the university to identify possible indicators of first-year students’ non-engagement in the first semester and their possible impact on the first semester academic performance. The findings suggest that there are indeed some indicators that predict Grade Point Average at the end of the first semester.
To assess whether induced vitellogenesis in longfinned eels mimics that in naturally maturing conspecifics, female eels were artificially matured and steroid hormone status and oocyte cytology during oogenesis were evaluated. Successful induction of vitellogenesis was evident from the presence of yolk granules in the ooplasm of salmon pituitary homogenate (SPH)-injected, but not saline-, 17-hydroxyprogesterone-, and/or gonadotropin-releasing hormone-treated fish. In SPH-treated females, the migratory nucleus stage was reached after 33-53 days, followed by ovulation around 30 hours after induction of final maturation and ovulation. Only a portion of the germ cells matured, although resumption of vitellogenesis was seen in the majority of oocytes. In contrast, in ovaries of saline-injected controls, the most advanced oocytes were early vitellogenic. Atretic follicles were observed in ovaries of all eels, but abundance was greater in controls than in SPH-treated fish. SPH injections elevated plasma levels of estradiol-17beta and androgens, but not pregnenes, from within three days of treatment. Our results indicate that sex steroid levels in midvitellogenic hormone-treated females are similar to those in wild midvitellogenic females. In contrast, differences in yolk morphology of midvitellogenic follicles were seen between SPH-treated and wild females, especially in the second crop of midvitellogenic-sized oocytes measuring 300-400 microm in diameter. We discuss whether the observed differences affect egg quality, and perhaps explain the short life span of captive-bred eel larvae. J. Exp. Zool. 289:119-129, 2001.
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