SELECTION AND BODY SIZE IN DROSOPHILA PSEUDOOBSCURA AT DIFFERENT TEMPERATURES

Genetics ◽  
1962 ◽  
Vol 47 (2) ◽  
pp. 209-222 ◽  
Author(s):  
Marvin Druger
1963 ◽  
Vol 4 (1) ◽  
pp. 104-131 ◽  
Author(s):  
A. M. McFarquhar ◽  
Forbes W. Robertson

1. The paper described an attempt to see whether differences in co-adaptation between populations of Drosophila subobscura are related to the distance between them. The mean and the variance of body-size, development time and survival were recorded on parent populations and the F1 and F2 of various crosses to test for heterosis in the F1 and decline in performance or greater variance in the F2, which might indicate the break-up of co-adapted gene arrays. Comparisons were carried out at different temperatures and on a variety of larval diets, especially sub-optimal ones in which the larvae were grown on synthetic media. A large number of wild flies were caught at sites separated by about 10 miles along a transect of southern Scotland; these comprised one series of comparisons. For more distant crosses flies were caught at sites in southern England, Denmark, Switzerland and Israel.2. There were well-defined differences in body-size, and, to a lesser degree, development time between populations from more widely separated localities and these showed evidence of a cline, northern populations having larger body-size. The difference in size between the Scottish and Isreal populations is about 20%.3. There was no evidence of differences in co-adaptation between populations even in crosses between populations from sites as far apart as Scotland and Israel. The F1's were always close to the mid-parent values and there was no evidence of breakdown in the F2 nor of increased variability.4. There was hardly any evidence of gene-environment interaction either with respect to different diets or to different temperatures.5. Records of body-size on flies caught in the wild showed that they are extremely variable, indicating great variation in larval nutrition. Under natural condition stability of growth in body-size is conspicuously lacking in this species.6. An additional test of co-adaptation was based on the between-family variance of abdominal bristle number of intra- and inter-population matings in the two most widely separated populations. There was no evidence of greater variance in the inter-population series.7. To test for possible differences in breeding structure, the response to inbreeding was determined for two widely separated populations of D. subobscura and a long-established cage population of D. melanogaster, on an unrestricted larval diet and also on several different kinds of sub-optimal diets. There was little or no sign of consistent differences between the species in their response to inbreeding.8. This test revealed differences between the two species in their minimum requirements for particular nutrients. subobscura is less able than melanogaster to withstand lower levels of protein and survival is particularly reduced. On the other hand, melanogaster has a considerably higher requirement for choline. Where there are apparent differences between the species in the average effect of inbreeding, the inbreeding effect is greater on the relatively more sub-optimal diet.9. Comparison of the performance of the immediate descendants of wild flies with those derived from the same site, but kept in the laboratory for some twenty generations, failed to show any differences on several different diets and so there was no evidence that adaptation to laboratory conditions was important.10. The lack of evidence for co-adaptation apparently conflicts with what has been claimed for other species. Such differences are discussed.


2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Michelle L Taylor ◽  
Alison Skeats ◽  
Alastair J Wilson ◽  
Tom A R Price ◽  
Nina Wedell

1993 ◽  
Vol 62 (1) ◽  
pp. 63-75 ◽  
Author(s):  
M. D. Gebhardt ◽  
W. W. Anderson

SummaryWe measured temperature-dependent fertility selection on body size in Drosophila pseudoobscura in the laboratory. One hundred single females of each of the three karyotypes involving the ‘sexratio’ (SR) and the standard (ST) gene arrangement on the sex chromosome laid eggs at either 18 or 24°C. The experiment addressed the following hypotheses: (a) Fertility selection on body size is weaker at the higher temperature, explaining in part why genetically smaller flies appear to evolve in populations at warmer localities, (b) Homokaryotypic SR females are less fecund than homokaryotypic ST females, possibly mediated by the effect of body size on fertility, explaining the low frequencies of SR despite its strong advantage due to meiotic drive. The data were also expected to shed light on a mechanism for the evolution of plasticity of body size through fertility selection in environments with an unpredictable temperature regime. Hypothesis (a) was clearly refuted because phenotypically larger ST females had an even larger fertility surplus at the higher temperature and, more importantly, the genetic correlation between fertility and body size disappeared at the lower temperature. As to (b), we found that temperature affects fertility directly and indirectly through body size such that ST and SR females were about equally fecund at both temperatures, although different in size and size-adjusted fertility. We observed heterosis for both size and fertility, which might stabilize the polymorphism in nature. The reaction norms of body size to the temperature difference were steeper for ST females than for SR females, implying that fertility selection could change phenotypic plasticity of body size in a population. Selection on body size depended not only on the temperature, but also on the karyotypes, suggesting that models of phenotype evolution using purely phenotypic fitness functions may often be inadequate.


1968 ◽  
Vol 12 (3) ◽  
pp. 317-330 ◽  
Author(s):  
Wyatt W. Anderson

Body size in Drosophila pseudoobscura is a continuously varying character with a high heritability; it is almost certainly related to fitness. Natural populations of D. pseudoobscura from Canada to Mexico have been sampled and found to vary geographically in body size. The geographic variation for the genes determining size is to some extent correlated with the physiographic division of the West. The populations from the Pacific coast have genetically smaller flies than do those from the interior provinces. Experimental populations derived from the samples of seven widely separated natural populations were crossed to yield F1 and F2 hybrid generations. Body size in the F1's varied irregularly, while the F2's showed a consistent ‘breakdown’, the F2's being significantly smaller than their F1 parents. The F1's were significantly less variable than their parents, while the F2's were significantly more variable than their parents of the F1 generation. The natural populations possess coadapted genetic systems, with genes mutually adjusted by selection for favorable interactions. Recombination disrupted the balanced genic complexes to give the F2 breakdown and the increased F2 variability. D. pseudoobscura differs from D. subobscura in showing the effects expected in crosses between coadapted systems. This species difference lends additional support to the hypothesis that the gene pools of these two successful species respond in different ways to environmental variation. The gene pool of D. pseudoobscura is flexible and changes readily, while that of D. subobscura is relatively rigid.


2003 ◽  
Vol 60 (8) ◽  
pp. 929-937 ◽  
Author(s):  
Myron A Peck ◽  
Lawrence J Buckley ◽  
David A Bengtson

We examined the effects of body size (3–13 cm total length) and temperature (4.5, 8.0, 12.0, and 15.5 °C) on routine (RR) and feeding (RSDA) energy losses by laboratory-reared, young-of-year juvenile Atlantic cod (Gadus morhua). The magnitude of the effect of temperature on RR, expressed via the Q10, was nonlinear. Q10 values were greatest at temperatures between 4.5 and 8.0 °C and were lowest between 8.0 and 15.5 °C, with larger fish tending to exhibit the greatest change in RR irrespective of the temperature combination. Energy losses resulting from RSDA were ~4% of consumed energy, a value less than half that estimated for larger, year-1+ juvenile cod fed similar-sized rations. Data from this and other studies were combined to generate an equation estimating routine energy loss at different temperatures and body sizes for cod. The equation describes RR over the eight orders of magnitude difference in body size from young larvae to adults within a range of environmental temperatures experienced by this species on Georges Bank and other areas in the North Atlantic.


2021 ◽  
Author(s):  
Muhammad I. Maulana ◽  
Joost A.G. Riksen ◽  
Basten L. Snoek ◽  
Jan E. Kammenga ◽  
Mark G. Sterken

Most ectotherms obey the temperature-size rule, meaning they grow larger in a colder environment. This raises the question of how the interplay between genes and temperature affect the body size of ectotherms. Despite the growing body of literature on the physiological life-history and molecular genetic mechanism underlying the temperature-size rule, the overall genetic architecture orchestrating this complex phenotype is not yet fully understood. One approach to identify genetic regulators of complex phenotypes is Quantitative Trait Locus (QTL) mapping. Here, we explore the genetic architecture of body size phenotypes, in different temperatures using Caenorhabditis elegans as a model ectotherm. We used 40 recombinant inbred lines (RILs) derived from N2 and CB4856, which were reared at four different temperatures (16oC, 20oC, 24oC, and 26oC) and measured at two developmental stages (L4 and adult). The animals were measured for body length, width at vulva, body volume, length/width ratio, and seven other body-size traits. The genetically diverse RILs varied in their body-size phenotypes with heritabilities ranging from 0.0 to 0.99. We detected 18 QTL underlying the body-size phenotypes across all treatment combinations, with the majority clustering on chromosome X. We hypothesize that the chromosome X QTL could result from a known pleiotropic regulator - npr-1 - known to affect the body size of C. elegans through behavioural changes. In conclusion, our findings shed more light on multiple loci affecting body size plasticity and allow for a more refined analysis of the temperature-size rule.


2017 ◽  
Author(s):  
K. E. Fussmann ◽  
B. Rosenbaum ◽  
U. Brose ◽  
B.C. Rall

AbstractGlobal change is heating up ecosystems fuelling biodiversity loss and species extinctions. High-trophic-level predators are especially prone to extinction due to an energetic mismatch between increasing feeding rates and metabolism with warming. Different adaptation mechanisms such as decreasing body size to reduce energy requirements (morphological response) as well as direct effects of adaptation to feeding parameters (physiological response) have been proposed to overcome this problem. Here, we use protist-bacteria microcosm experiments to show how those adaptations may have the potential to buffer the impact of warming on predator-prey interactions. After adapting the ciliate predator Tetrahymena pyriformis to three different temperatures (15°C, 20°C and 25°C) for approximately 20 generations we conducted functional response experiments on bacterial prey along an experimental temperature gradient (15°C, 20°C and 25°C). We found an increase of maximum feeding rates and half-saturation densities with rising experimental temperatures. Adaptation temperature had on average slightly negative effects on maximum feeding rates, but maximum feeding rates increased more strongly with rising experimental temperature in warm adapted predators than in cold adapted predators. There was no effect of adaptation temperature on half-saturation densities characterising foraging efficiency. Besides the mixed response in functional response parameters, predators also adapted by decreasing body size. As smaller predators need less energy to fulfil their energetic demands, maximum feeding rates relative to the energetic demands increased slightly with increased adaptation temperature. Accordingly, predators adapted to 25°C showed the highest feeding rates at 25°C experimental temperature, while predators adapted to 15°C showed the highest maximum feeding rate at 15°C. Therefore, adaptation to different temperatures potentially avoids an energetic mismatch with warming. Especially a shift in body size with warming additionally to an adaptation of physiological parameters potentially helps to maintain a positive energy balance and prevent predator extinction with rising temperatures.


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