scholarly journals Sexually Different Growth Histories of the American Eel in Four Rivers in Maine

Author(s):  
Kenneth Oliveira ◽  
James D. McCleave
Keyword(s):  
Author(s):  
Sam C. Chin ◽  
John Waldman ◽  
Mike Bednarski ◽  
Merry Camhi ◽  
Jake LaBelle ◽  
...  

2009 ◽  
Vol 16 (4) ◽  
pp. 306-314 ◽  
Author(s):  
H. M. LAMSON ◽  
D. K. CAIRNS ◽  
J.-C. SHIAO ◽  
Y. IIZUKA ◽  
W.-N. TZENG

1983 ◽  
Vol 245 (1) ◽  
pp. R32-R37
Author(s):  
P. J. Walsh ◽  
T. W. Moon

The effects of acclimation temperature and acute temperature changes on the intracellular pH (pHi) of hepatocytes isolated from the American eel, Anguilla rostrata, were studied by the measurement of the distribution ratio of dimethyloxizolidinedione (DMO). Varying the concentration of DMO (10(-7) to 10(-4) M) did not affect estimates of pHi, indicating that DMO acts as an ideal pHi probe in eel hepatocytes. In vitro studies yielded values of liver cell pHi identical to those previously measured in vivo (in vitro pHi = 7.556 +/- 0.010; in vivo pHi = 7.570 +/- 0.049 at 20 degrees C); hepatocyte pHi varied inversely with acclimation temperature (5-20 degrees C) in a manner consistent with alphastat regulation (delta pH/delta T = -0.0182 +/- 0.021). During acute temperature increases (5-20 degrees C) and decreases (20-5 degrees C) hepatocytes regulated pHi to the appropriate (acclimated) value within 30-45 min posttransfer under conditions of constant medium pH (pHe). The effects of medium pH were also studied, and although patterns of pHi regulation differed between 5 and 20 degrees C cells, a pHi difference consistent with alphastat regulation was maintained between 5 and 20 degrees C cells over the pHe range 7.8-8.3.


2018 ◽  
Vol 35 ◽  
pp. 159-168 ◽  
Author(s):  
CK Elvidge ◽  
MI Ford ◽  
TC Pratt ◽  
KE Smokorowski ◽  
M Sills ◽  
...  

2010 ◽  
Vol 88 (11) ◽  
pp. 1121-1128 ◽  
Author(s):  
K. Oliveira ◽  
W. E. Hable

Spawning for the American eel ( Anguilla rostrata (Le Sueur, 1817)) takes place in secretive locations within the Sargasso Sea, which has thus far prevented investigations of gametogenesis and early development in this ecologically and commercially important species. Attempts to induce maturation and reproduction in this species have been few and have produced limited results, with a single report of the production of gastrula-stage embryos. Here we report the successful maturation of female American eels. Maturation occurred within 13 weeks and ovulation was induced with a single injection of 17α,20β-dihydroxy-4-pregnen-3-one (DHP). Following in vitro fertilization, embryogenesis through hatching was observed and larvae were maintained for up to 6 days. We show that a crucial factor for successful fertilization is the stage of the oocyte at the time of induced ovulation. Oocytes that had not reached the migratory nucleus stage, or had passed this stage, were not successfully fertilized. These findings demonstrate that American eel can reproduce in the laboratory and previously untestable hypotheses pertaining to the developmental biology of this elusive species can now be explored.


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