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      Feeding Preference of Crapemyrtle Bark Scale ( Acanthococcus lagerstroemiae) on Different Species

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          Abstract

          Crapemyrtle bark scale (CMBS; Acanthococcus lagerstroemiae) is an exotic pest species that causes aesthetic and economic damage to crapemyrtles and poses potential threats to other horticultural crops in the United States. Although previous studies reported the infestation of CMBS on several alternative hosts across multiple families in Asia, its potential threats to other documented alternative hosts remain elusive and yet to be confirmed. In this study, feeding preference studies of CMBS were conducted on forty-nine plant species and cultivars in 2016 and 2019, in order to gain insight into the expansion of CMBS distribution in the United States, as well as other regions of the world. The infestations of CMBS were confirmed on apple ( Malus domestica), Chaenomeles speciosa, Disopyros rhombifolia, Heimia salicifolia, Lagerstroemia ‘Spiced Plum’, M. angustifolia, and twelve out of thirty-five pomegranate cultivars. However, the levels of CMBS infestation on these test plant hosts in this study is very low compared to Lagerstroemia, and may not cause significant damage. No sign of CMBS infestation was observed on Rubus ‘Arapaho’, R. ‘Navaho’, R. idaeus ‘Dorman Red’, R. fruticosus, B. microphylla var. koreana × B. sempervirens, B. harlandii, or D. virginiana.

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          Most cited references72

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          Host Selection in Phytophagous Insects

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            Phloem amino acids and the host plant range of the polyphagous aphid, Aphis fabae

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              Are adaptation costs necessary to build up a local adaptation pattern?

              Background Ecological specialization is pervasive in phytophagous arthropods. In such specialization mode, limits to host range are imposed by trade-offs preventing adaptation to several hosts. The occurrence of such trade-offs is inferred by a pattern of local adaptation, i.e., a negative correlation between relative performance on different hosts. Results To establish a causal link between local adaptation and trade-offs, we performed experimental evolution of spider mites on cucumber, tomato and pepper, starting from a population adapted to cucumber. Spider mites adapted to each novel host within 15 generations and no further evolution was observed at generation 25. A pattern of local adaptation was found, as lines evolving on a novel host performed better on that host than lines evolving on other hosts. However, costs of adaptation were absent. Indeed, lines adapted to tomato had similar or higher performance on pepper than lines evolving on the ancestral host (which represent the initial performance of all lines) and the converse was also true, e.g. negatively correlated responses were not observed on the alternative novel host. Moreover, adapting to novel hosts did not result in decreased performance on the ancestral host. Adaptation did not modify host ranking, as all lines performed best on the ancestral host. Furthermore, mites from all lines preferred the ancestral to novel hosts. Mate choice experiments indicated that crosses between individuals from the same or from a different selection regime were equally likely, hence development of reproductive isolation among lines adapted to different hosts is unlikely. Conclusion Therefore, performance and preference are not expected to impose limits to host range in our study species. Our results show that the evolution of a local adaptation pattern is not necessarily associated with the evolution of an adaptation cost.
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                Author and article information

                Journal
                Insects
                Insects
                insects
                Insects
                MDPI
                2075-4450
                28 June 2020
                July 2020
                : 11
                : 7
                : 399
                Affiliations
                [1 ]Department of Horticultural Sciences, Texas A&M University, College Station, TX 77843, USA; fushe001@ 123456tamu.edu (R.X.); bin.wu@ 123456tamu.edu (B.W.); haijiedou@ 123456outlook.com (H.D.)
                [2 ]Department of Science & Technology Development, Beijing Industrial Technology Research Institute, No.5, Xingguang 4th Ave, Tongzhou District, Beijing 101111, China
                [3 ]College of Forestry, Nanjing Forestry University, 159 Longpan Rd., Nanjing 210037, China; ankar_liu@ 123456163.com
                [4 ]Department of Environmental Horticulture, University of Florida/IFAS North Florida Research and Education Center, Quincy, FL 32351, USA; gwknox@ 123456ufl.edu
                [5 ]Department of Biology, Texas A&M University, College Station, TX 77840, USA
                [6 ]Department of Horticultural Sciences, Texas A&M AgriLife Extension Service, College Station, TX 77843, USA
                Author notes
                [* ]Correspondence: hqin@ 123456bio.tamu.edu (H.Q.); mgu@ 123456tamu.edu (M.G.); Tel.: +1-979-458-0512 (H.Q.); +1-979-845-8567 (M.G.)
                Author information
                https://orcid.org/0000-0001-5285-5439
                Article
                insects-11-00399
                10.3390/insects11070399
                7412028
                32605244
                4ad26250-61d2-4605-a5ff-9e869ac8e59f
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 02 June 2020
                : 25 June 2020
                Categories
                Article

                lagerstroemia,host range,pomegranates,apple,scale insect,exotic pest

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