scholarly journals Rates and Patterns of Laboratory Adaptation in (Mostly) Insects

2018 ◽  
Vol 111 (2) ◽  
pp. 501-509 ◽  
Author(s):  
Ary A Hoffmann ◽  
Perran A Ross
2018 ◽  
Vol 12 (3) ◽  
pp. 572-586 ◽  
Author(s):  
Perran A. Ross ◽  
Nancy M. Endersby‐Harshman ◽  
Ary A. Hoffmann

1999 ◽  
Vol 36 (4) ◽  
pp. 157-160 ◽  
Author(s):  
Pierre-Marie Sarradin ◽  
Nadine Le Bris ◽  
Jean-Claude Caprais ◽  
Dominique Birot

2004 ◽  
Vol 94 (6) ◽  
pp. 517-524 ◽  
Author(s):  
A. Meats ◽  
H.M. Holmes ◽  
G.L. Kelly

AbstractA significant reduction in age of mating occurred during the first four generations (G1–G4) of laboratory adaptation of wildBactrocera tryoni(Froggatt) and this was associated with the earlier attainment of peak egg load although no significant differences were detected in the peak egg load itself. A long term laboratory (LTL) strain had a significantly earlier mating age and higher peak egg load than flies of wild origin or those from the first four laboratory generations. The amount of protein consumed by females in the first week of adult life was significantly higher in the LTL strain than in flies of wild origin or G1–G4 but there were no significant changes (or only slight changes) with laboratory adaptation in the amounts of protein consumed up to the ages of mating and peak egg load. Laboratory adaptation resulted in no significant changes in egg size, egg dry weight, puparial fresh weight and the dry weight of newly emerged females. The large increase in fecundity with laboratory adaptation is associated with a 4- to 5-fold increase in the rate of conversion of dietary protein to eggs (i.e. eggs produced per mg of protein consumed).


PLoS ONE ◽  
2015 ◽  
Vol 10 (11) ◽  
pp. e0142997 ◽  
Author(s):  
Owen P. Leiser ◽  
Eric D. Merkley ◽  
Brian H. Clowers ◽  
Brooke L. Deatherage Kaiser ◽  
Andy Lin ◽  
...  

1996 ◽  
Vol 74 (1) ◽  
pp. 164-170 ◽  
Author(s):  
Robin J. Stuart ◽  
Randy Gaugler

Laboratory culture can have detrimental effects on populations through adverse environmental conditions such as poor nutrition or disease, or through genetic effects such as inbreeding depression, founder effect, genetic drift, or laboratory adaptation. We tested for laboratory effects on the entomopathogenic nematode Steinernema glaseri (Steiner) by forming a genetically diverse base population from a series of field isolates and rearing several independent lines through 12 cycles of laboratory culture, using larvae of the greater wax moth, Galleria mellonella (L.), or the Japanese beetle, Popillia japonica Newman, as hosts. Laboratory bioassays based on G. mellonella indicated that lines maintained with large breeding populations did not deteriorate but often showed significant increases in infectivity (15.3–48.0%), proportion of males (12.2–36.1%), and reproductive potential (39.0–160.4%). Lines reared on P. japonica larvae responded similarly to lines reared on G. mellonella but showed higher levels of reproductive potential. Two of three lines subjected to initial genetic bottlenecks to test for founder effects differed from other lines by showing very high infectivity but little change in sex ratio or reproductive potential. These results demonstrate that laboratory adaptation can produce dramatic changes in important biological attributes of these nematodes, but that a lack of genetic variation associated with founder effects can impede this process. Laboratory adaptation should be considered a potent factor when designing, interpreting, and comparing studies of this important group of biological control organisms.


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