Phenotypic and Genetic Covariance Structure in Milkweed Bug Life History Traits

1982 ◽  
pp. 177-185 ◽  
Author(s):  
Joseph P. Hegmann ◽  
Hugh Dingle
Keyword(s):  
Life History ◽  
Life History Traits ◽  
Covariance Structure ◽  
Genetic Covariance ◽  
Milkweed Bug

scholarly journals The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect

2018 ◽  
Vol 31 (6) ◽  
pp. 853-865 ◽  
Author(s):  
Szymon Sniegula ◽  
Maria J. Golab ◽  
Szymon M. Drobniak ◽  
Frank Johansson
Keyword(s):  
Life History ◽  
Life History Traits ◽  
Genetic Variance ◽  
Genetic Covariance ◽  
The North

scholarly journals Genetic variation and covariation of aphid life-history traits across unrelated host plants

2008 ◽  
Vol 98 (6) ◽  
pp. 543-553 ◽  
Author(s):  
C. Vorburger ◽  
N. Ramsauer
Keyword(s):  
Genetic Variation ◽  
Life History ◽  
Host Plants ◽  
Life History Theory ◽  
Life History Traits ◽  
Genetic Correlations ◽  
Covariance Structure ◽  
Clonal Variation ◽  
Common Lambsquarters ◽  
Trade Offs

AbstractA central paradigm of life-history theory is the existence of resource mediated trade-offs among different traits that contribute to fitness, yet observations inconsistent with this tenet are not uncommon. We previously found a clonal population of the aphid Myzus persicae to exhibit positive genetic correlations among major components of fitness, resulting in strong heritable fitness differences on a common host. This raises the question of how this genetic variation is maintained. One hypothesis states that variation for resource acquisition on different hosts may override variation for allocation, predicting strong fitness differences within hosts as a rule, but changes in fitness hierarchies across hosts due to trade-offs. Therefore, we carried out a life-table experiment with 17 clones of M. persicae, reared on three unrelated host plants: radish, common lambsquarters and black nightshade. We estimated the broad-sense heritabilities of six life-history traits on each host, the genetic correlations among traits within hosts, and the genetic correlations among traits on different hosts (cross-environment genetic correlations). The three plants represented radically different environments with strong effects on performance of M. persicae, yet we detected little evidence for trade-offs. Fitness components were positively correlated within hosts but also between the two more benign hosts (radish and lambsquarters), as well as between those and another host tested earlier. The comparison with the most stressful host, nightshade, was hampered by low survival. Survival on nightshade also exhibited genetic variation but was unrelated to fitness on other hosts. Acknowledging that the number of environments was necessarily limited in a quantitative genetic experiment, we suggest that the rather consistent fitness hierarchies across very different plants provided little evidence to support the idea that the clonal variation for life-history traits and their covariance structure are maintained by strong genotype×environment interactions with respect to hosts. Alternative explanations are discussed.

Prey tell: what quillback rockfish early life history traits reveal about their survival in encounters with juvenile coho salmon

2020 ◽  
Vol 650 ◽  
pp. 7-18 ◽  
Author(s):  
HW Fennie ◽  
S Sponaugle ◽  
EA Daly ◽  
RD Brodeur
Keyword(s):  
Life History ◽  
Early Life ◽  
Life History Traits ◽  
Direct Evidence ◽  
Coho Salmon ◽  
Larval Fish ◽  
Early Life History ◽  
In The Wild ◽  
Otolith Microstructure Analysis ◽  
Pelagic Juvenile

Predation is a major source of mortality in the early life stages of fishes and a driving force in shaping fish populations. Theoretical, modeling, and laboratory studies have generated hypotheses that larval fish size, age, growth rate, and development rate affect their susceptibility to predation. Empirical data on predator selection in the wild are challenging to obtain, and most selective mortality studies must repeatedly sample populations of survivors to indirectly examine survivorship. While valuable on a population scale, these approaches can obscure selection by particular predators. In May 2018, along the coast of Washington, USA, we simultaneously collected juvenile quillback rockfish Sebastes maliger from both the environment and the stomachs of juvenile coho salmon Oncorhynchus kisutch. We used otolith microstructure analysis to examine whether juvenile coho salmon were age-, size-, and/or growth-selective predators of juvenile quillback rockfish. Our results indicate that juvenile rockfish consumed by salmon were significantly smaller, slower growing at capture, and younger than surviving (unconsumed) juvenile rockfish, providing direct evidence that juvenile coho salmon are selective predators on juvenile quillback rockfish. These differences in early life history traits between consumed and surviving rockfish are related to timing of parturition and the environmental conditions larval rockfish experienced, suggesting that maternal effects may substantially influence survival at this stage. Our results demonstrate that variability in timing of parturition and sea surface temperature leads to tradeoffs in early life history traits between growth in the larval stage and survival when encountering predators in the pelagic juvenile stage.

Life History Traits in a Population of Pelobates syriacus (Boettger, 1889) from Turkey

2020 ◽  
Vol 27 (4) ◽  
pp. 195-200
Author(s):  
Ufuk Bülbül ◽  
Halime Koç ◽  
Yasemin Odabaş ◽  
Ali İhsan Eroğlu ◽  
Muammer Kurnaz ◽  
...  
Keyword(s):  
Life History ◽  
Age Structure ◽  
Life History Traits ◽  
Spadefoot Toad ◽  
Males And Females

Age structure of the eastern spadefoot toad, Pelobates syriacus from the Kızılırmak Delta (Turkey) were assessed using phalangeal skeletochronology. Snout-vent length (SVL) ranged from 42.05 to 86.63 mm in males and 34.03 to 53.27 mm in females. Age of adults ranged from 2 to 8 years in males and 3 to 5 years in females. For both sexes, SVL was significantly correlated with age. Males and females of the toads reached maturity at 2 years of age.

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