Embryonic development and hatchability of red‐spotted grouper ( Epinephelus akaara ) ♀ × giant grouper ( E. lanceolatus ) ♂ hybrid at three incubation temperatures

2019 ◽  
Vol 50 (11) ◽  
pp. 3477-3481
Author(s):  
Choong Hwan Noh ◽  
Min Joo Kang ◽  
Sung Jin Yoon
Zygote ◽  
2016 ◽  
Vol 24 (5) ◽  
pp. 733-741
Author(s):  
Samuel Louzada Pereira ◽  
Dalcio Ricardo de Andrade ◽  
Marcella Costa Radael ◽  
João Carlos Fosse Filho ◽  
Rafael Vieira de Azevedo ◽  
...  

SummaryTemperature is an environmental factor that influences the development of fish, and when changed abruptly can lead to high mortality. Some species of fish are influenced by this factor, exhibiting a longer time for embryonic development and time to first feeding. This study aims to evaluate the effect of water temperature on embryonic and larval development up to first feeding, to describe the time in hours post fertilization (hpf) of the emergence of different structures and to determine the best hatching rate and survival of animals under different treatments. Five different egg incubation temperatures were used (24, 26, 28, 30 or 32°C, respectively). The eggs were observed at regular intervals of 30 min up to 24 h, every 2 h until 48 h and every 4 h until the display of first feeding in all treatments. Embryonic development was longer for eggs incubated at 24°C and the best results for hatching rate and survival of spawning efficiency were at 28°C. We recommend that incubation of Trichogaster leeri eggs is carried out at 28°C up to the first feeding of larvae.


Aquaculture ◽  
2006 ◽  
Vol 259 (1-4) ◽  
pp. 243-248 ◽  
Author(s):  
Xin-Ping Zhu ◽  
Chen-Qing Wei ◽  
Wei-Hua Zhao ◽  
He-Jun Du ◽  
Yong-Le Chen ◽  
...  

2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.


2014 ◽  
Vol 47 (06) ◽  
Author(s):  
N Bergemann ◽  
K Boyle ◽  
WE Paulus

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