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      Heritability and Evolutionary Potential Drive Cold Hardiness in the Overwintering Ophraella communa Beetles

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          Abstract

          Chill tolerance plays a crucial role that allows insect species to adapt to cold environments. Two Chinese geographical populations (Laibin and Yangzhou populations) were selected to understand the chill resistance and evolutionary potential in the Ophraella communa, a biological control agent of the invasive common ragweed, Ambrosia artemisiifolia. Super-cooling point assays, knockdown tests under static low-temperature conditions and determination of glycerol content were studied. ANOVAs indicated significant differences regarding chill coma recovery time, super-cooling point, and glycerol content across populations and sexes. The narrow-sense heritability ( h 2) estimates of cold resistance based on a parental half-sibling breeding design ranged from 0.39 to 0.53, and the h 2 value was significantly higher in the Yangzhou population than in the Laibin population. Additive genetic variances were significantly different from zero for cold tolerance. The Yangzhou population of O. communa has a strong capability to quickly gain resistance to cold. We conclude that the O. communa beetle has a plasticity that can provide cold resistance in the changing climate conditions.

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          Most cited references49

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          Comparing evolvability and variability of quantitative traits.

          D. Houle (1992)
          There are two distinct reasons for making comparisons of genetic variation for quantitative characters. The first is to compare evolvabilities, or ability to respond to selection, and the second is to make inferences about the forces that maintain genetic variability. Measures of variation that are standardized by the trait mean, such as the additive genetic coefficient of variation, are appropriate for both purposes. Variation has usually been compared as narrow sense heritabilities, but this is almost always an inappropriate comparative measure of evolvability and variability. Coefficients of variation were calculated from 842 estimates of trait means, variances and heritabilities in the literature. Traits closely related to fitness have higher additive genetic and nongenetic variability by the coefficient of variation criterion than characters under weak selection. This is the reverse of the accepted conclusion based on comparisons of heritability. The low heritability of fitness components is best explained by their high residual variation. The high additive genetic and residual variability of fitness traits might be explained by the great number of genetic and environmental events they are affected by, or by a lack of stabilizing selection to reduce their phenotypic variance. Over one-third of the quantitative genetics papers reviewed did not report trait means or variances. Researchers should always report these statistics, so that measures of variation appropriate to a variety of situations may be calculated.
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            Adaptation of Drosophila to temperature extremes: bringing together quantitative and molecular approaches

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              Heritability is not Evolvability

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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                05 June 2018
                2018
                : 9
                : 666
                Affiliations
                [1] 1State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences , Beijing, China
                [2] 2Key Laboratory of Biosafety, Ministry of Environmental Protection , Nanjing, China
                [3] 3Nanjing Institute of Environmental Sciences, Ministry of Environmental Protection , Nanjing, China
                [4] 4Guangxi Key Laboratory of Biology for Crop Diseases and Insect Pests, Institute of Plant Protection, Guangxi Academy of Agricultural Sciences , Nanning, China
                Author notes

                Edited by: Su Wang, Beijing Academy of Agriculture and Forestry Sciences, China

                Reviewed by: Dandan Wei, Southwest University, China; Shannon Bryn Olsson, National Centre for Biological Sciences, India

                *Correspondence: Zhongshi Zhou, zhongshizhou@ 123456yahoo.com

                These authors have contributed equally to this work as joint first authors.

                This article was submitted to Invertebrate Physiology, a section of the journal Frontiers in Physiology

                Article
                10.3389/fphys.2018.00666
                5996086
                48056ef4-ab64-4ef5-aa4f-0162222099c4
                Copyright © 2018 Zhao, Ma, Chen, Wan, Guo and Zhou.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 07 March 2018
                : 14 May 2018
                Page count
                Figures: 2, Tables: 1, Equations: 3, References: 64, Pages: 9, Words: 0
                Funding
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 31322046
                Award ID: 31672089
                Categories
                Physiology
                Original Research

                Anatomy & Physiology
                ophraella communa,heritability,cold hardiness,super cooling point,glycerol content,chill coma recovery time

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