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      Life‐history traits of the Whiting polyploid line of the parasitoid Nasonia vitripennis

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          Abstract

          In hymenopterans, males are normally haploid (1n) and females diploid (2n), but individuals with divergent ploidy levels are frequently found. In species with ‘complementary sex determination’ (CSD), increasing numbers of diploid males that are often infertile or unviable arise from inbreeding, presenting a major impediment to biocontrol breeding. Non‐CSD species, which are common in some parasitoid wasp taxa, do not produce polyploids through inbreeding. Nevertheless, polyploidy also occurs in non‐CSD Hymenoptera. As a first survey on the impacts of inbreeding and polyploidy of non‐CSD species, we investigate life‐history traits of a long‐term laboratory line of the parasitoid Nasonia vitripennis (Walker) (Hymenoptera: Pteromalidae) (‘Whiting polyploid line’) in which polyploids of both sexes (diploid males, triploid females) are viable and fertile. Diploid males produce diploid sperm and virgin triploid females produce haploid and diploid eggs. We found that diploid males did not differ from haploid males with respect to body size, progeny size, mate competition, or lifespan. When diploid males were mated to many females (without accounting for mating order), the females produced a relatively high proportion of male offspring, possibly indicating that these males produce less sperm and/or have reduced sperm functionality. In triploid females, parasitization rate and fecundity were reduced and body size was slightly increased, but there was no effect on lifespan. After one generation of outbreeding, lifespan as well as parasitization rate were increased, and a body size difference was no longer apparent. This suggests that outbreeding has an effect on traits observed in an inbred polyploidy background. Overall, these results indicate some phenotypic detriments of non‐CSD polyploids that must be taken into account in breeding.

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          Most cited references51

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          Polyploid incidence and evolution.

          Changes in ploidy occurred early in the diversification of some animal and plant lineages and represent an ongoing phenomenon in others. While the prevalence of polyploid lineages indicates that this phenomenon is a common and successful evolutionary transition, whether polyploidization itself has a significant effect on patterns and rates of diversification remains an open question. Here we review evidence for the creative role of polyploidy in evolution. We present new estimates for the incidence of polyploidy in ferns and flowering plants based on a simple model describing transitions between odd and even base chromosome numbers. These new estimates indicate that ploidy changes may represent from 2 to 4% of speciation events in flowering plants and 7% in ferns. Speciation via polyploidy is likely to be one of the more predominant modes of sympatric speciation in plants, owing to its potentially broad-scale effects on gene regulation and developmental processes, effects that can produce immediate shifts in morphology, breeding system, and ecological tolerances. Theoretical models support the potential for increased adaptability in polyploid lineages. The evidence suggests that polyploidization can produce shifts in genetic systems and phenotypes that have the potential to result in increased evolutionary diversification, yet conclusive evidence that polyploidy has changed rates and patterns of diversification remains elusive.
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            The state of commercial augmentative biological control: plenty of natural enemies, but a frustrating lack of uptake

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              Sex determination in the hymenoptera.

              The dominant and ancestral mode of sex determination in the Hymenoptera is arrhenotokous parthenogenesis, in which diploid females develop from fertilized eggs and haploid males develop from unfertilized eggs. We discuss recent progress in the understanding of the genetic and cytoplasmic mechanisms that make arrhenotoky possible. The best-understood mode of sex determination in the Hymenoptera is complementary sex determination (CSD), in which diploid males are produced under conditions of inbreeding. The gene mediating CSD has recently been cloned in the honey bee and has been named the complementary sex determiner. However, CSD is only known from 4 of 21 hymenopteran superfamilies, with some taxa showing clear evidence of the absence of CSD. Sex determination in the model hymenopteran Nasonia vitripennis does not involve CSD, but it is consistent with a form of genomic imprinting in which activation of the female developmental pathway requires paternally derived genes. Some other hymenopterans are not arrhenotokous but instead exhibit thelytoky or paternal genome elimination.
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                Author and article information

                Contributors
                k.leung@rug.nl
                Journal
                Entomol Exp Appl
                Entomol. Exp. Appl
                10.1111/(ISSN)1570-7458
                EEA
                Entomologia Experimentalis et Applicata
                John Wiley and Sons Inc. (Hoboken )
                0013-8703
                1570-7458
                17 July 2019
                July 2019
                : 167
                : 7 , Next Generation Biological Control ( doiID: 10.1111/eea.v167.7 )
                : 655-669
                Affiliations
                [ 1 ] Groningen Institute for Evolutionary Life Sciences University of Groningen PO Box 11103 9700 CC Groningen The Netherlands
                Author notes
                [*] [* ] Correspondence: E‐mail: k.leung@ 123456rug.nl

                Author information
                https://orcid.org/0000-0002-1392-6203
                https://orcid.org/0000-0001-9838-9314
                Article
                EEA12808
                10.1111/eea.12808
                6774307
                31598002
                cad51399-2f50-40a5-885f-834d2c9f6c34
                © 2019 The Authors. Entomologia Experimentalis et Applicata published by John Wiley & Sons Ltd on behalf of Netherlands Entomological Society

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 February 2019
                Page count
                Figures: 4, Tables: 1, Pages: 15, Words: 10792
                Funding
                Funded by: Marie Curie Innovative Training Network BINGO
                Award ID: 641456
                Categories
                Special Issue: Next Generation Biological Control
                Special Issue: Next Generation Biological Control
                Original Articles
                Custom metadata
                2.0
                eea12808
                July 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.9 mode:remove_FC converted:01.10.2019

                diploid male,triploid female,fitness,body size,parasitization rate,mate competition,biocontrol,hymenoptera,pteromalidae

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