Effects of temperature and salinity on the hatch rate and survival of Australian bass (Macquaria novemaculeata) eggs and yolk-sac larvae

Aquaculture ◽  
1985 ◽  
Vol 47 (2-3) ◽  
pp. 239-244 ◽  
Author(s):  
E.J. Van Der Wal
1979 ◽  
Vol 111 (6) ◽  
pp. 665-673 ◽  
Author(s):  
M.K. Friesen ◽  
J.F. Flannagan ◽  
S.G. Lawrence

AbstractEggs of Hexagenia rigida McDunnough transferred directly from 20° to 36°, 32°, 28°, 24°, 20°, 16°, 12°, and 8 °C were monitored for start of hatch, hatching rate, success of hatch, and hatching period. Eggs did not hatch at 36 °C or 8 °C. There was a direct relationship between temperature and start of hatch (from day 7 at 32 °C to day 77 at 12 °C). Over 90% hatch occurred at all temperatures except 12 °C. Hatching periods ranged from about 6 days at the higher temperatures to over 80 days at 16 °C and 12 °C. Hatching occurred at 36 °C when eggs were transferred in increments of 4 °C every 2 days.Storage capabilities of eggs in "early", "middle", and "late" stages of embryonic development were tested at 12 °C and 8 °C using a direct or stepwise transfer method. Hatching parameters monitored were hatch rate, success of hatch, and hatching period up to 90% hatch of total number of eggs. Middle stage eggs transferred in a stepwise manner could be held at 8 °C for up to 52 weeks with least effect on hatching parameters. Middle and late stage eggs could be stored for up to 16 weeks at 8 °C using the direct transfer method, and early stage eggs, which were affected most by cold storage, could be held for 2 days at 12 °C with minimal effect on hatching parameters. The storage of eggs, shown here to be possible, is potentially useful for providing such material for bioassays throughout the year.


Aquaculture ◽  
2021 ◽  
Vol 537 ◽  
pp. 736502
Author(s):  
Yuzo R. Yanagitsuru ◽  
Madison A. Main ◽  
Levi S. Lewis ◽  
James A. Hobbs ◽  
Tien-Chieh Hung ◽  
...  

Author(s):  
William P. Jollie

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.


Sign in / Sign up

Export Citation Format

Share Document