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      The Invasive Liriomyza huidobrensis (Diptera: Agromyzidae): Understanding Its Pest Status and Management Globally

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          Abstract

          Liriomyza huidobrensis (Blanchard) is native to South America but has expanded its range and invaded many regions of the world, primarily on flowers and to a lesser extent on horticultural product shipments. As a result of initial invasion into an area, damage caused is usually significant but not necessarily sustained. Currently, it is an economic pest in selected native and invaded regions of the world. Adults cause damage by puncturing abaxial and adaxial leaf surfaces for feeding and egg laying sites. Larvae mine the leaf parenchyma tissues which can lead to leaves drying and wilting. We have recorded 365 host plant species from 49 families and more than 106 parasitoid species. In a subset of the Argentinian data, we found that parasitoid community composition attacking L. huidobrensis differs significantly in cultivated and uncultivated plants. No such effect was found at the world level, probably due to differences in collection methods in the different references. We review the existing knowledge as a means of setting the context for new and unpublished data. The main objective is to provide an update of widely dispersed and until now unpublished data, evaluate dispersion of the leafminer and management strategies in different regions of the world, and highlight the need to consider the possible effects of climate change on further regional invasions or expansions.

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          Most cited references146

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          A meta-analysis of crop pest and natural enemy response to landscape complexity.

          Many studies in recent years have investigated the relationship between landscape complexity and pests, natural enemies and/or pest control. However, no quantitative synthesis of this literature beyond simple vote-count methods yet exists. We conducted a meta-analysis of 46 landscape-level studies, and found that natural enemies have a strong positive response to landscape complexity. Generalist enemies show consistent positive responses to landscape complexity across all scales measured, while specialist enemies respond more strongly to landscape complexity at smaller scales. Generalist enemy response to natural habitat also tends to occur at larger spatial scales than for specialist enemies, suggesting that land management strategies to enhance natural pest control should differ depending on whether the dominant enemies are generalists or specialists. The positive response of natural enemies does not necessarily translate into pest control, since pest abundances show no significant response to landscape complexity. Very few landscape-scale studies have estimated enemy impact on pest populations, however, limiting our understanding of the effects of landscape on pest control. We suggest focusing future research efforts on measuring population dynamics rather than static counts to better characterise the relationship between landscape complexity and pest control services from natural enemies. © 2011 Blackwell Publishing Ltd/CNRS.
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            Roles of thermal adaptation and chemical ecology in Liriomyza distribution and control.

            Many Liriomyza species are pests of agricultural and ornamental plants. In the past two decades, the occurrence and distribution of certain Liriomyza species have changed dramatically, leading to an extensive body of research papers. First, we review the association of thermal tolerance with population dynamics, geographic distribution, and species displacement. Differences in thermal tolerances between species result in their differential geographic locations and overwintering ranges. Displacements among Liriomyza species are associated with their temperature adaptation. We examine the chemical linkage of plants, Liriomyza, and their parasitoids. Chemical compounds from host and nonhost plants mediate the behavior of Liriomyza and their parasitoids. Liriomyza and their parasitoids use chemical cues to locate their hosts. Induced compounds can be used as attractants of parasitoids or repellents of Liriomyza. Thus, understanding the thermal tolerances and chemical ecology of Liriomyza may enable researchers to predict geographic distribution and to develop novel control strategies.
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              Early emergence in a butterfly causally linked to anthropogenic warming.

              There is strong correlative evidence that human-induced climate warming is contributing to changes in the timing of natural events. Firm attribution, however, requires cause-and-effect links between observed climate change and altered phenology, together with statistical confidence that observed regional climate change is anthropogenic. We provide evidence for phenological shifts in the butterfly Heteronympha merope in response to regional warming in the southeast Australian city of Melbourne. The mean emergence date for H. merope has shifted -1.5 days per decade over a 65-year period with a concurrent increase in local air temperatures of approximately 0.16°C per decade. We used a physiologically based model of climatic influences on development, together with statistical analyses of climate data and global climate model projections, to attribute the response of H. merope to anthropogenic warming. Such mechanistic analyses of phenological responses to climate improve our ability to forecast future climate change impacts on biodiversity.
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                Author and article information

                Journal
                J Insect Sci
                J. Insect Sci
                jis
                Journal of Insect Science
                Oxford University Press
                1536-2442
                January 2017
                28 February 2017
                28 February 2017
                : 17
                : 1
                : 28
                Affiliations
                [1 ]Department of Entomology, Agriculture Research Organization, Gilat Research Center, M.P. Negev 85280, Israel
                [3 ]Systematic Entomology Laboratory, USDA-ARS, Bldg 010A, BARC-W, 10300 Baltimore Ave, Beltsville, MD 20705
                [4 ]ARC-Vegetable and Ornamental Plants, Private Bag X293, Pretoria 0001, South Africa
                [5 ]Centro de Investigaciones Entomológicas de Córdoba – Instituto Multidisplinario de Biología Vegetal (CONICET–UNC), Av. Vélez Sársfield 1611-(X5016GCA), Córdoba, Argentina
                [6 ]Laboratorio de Ecologia Molecular, Department de Entomologia e Acarologia, ESALQ/Universidade de Sao Paulo, Av. Padua Dias, 11, Piracicaba-SP 13418-900, Brazil
                [7 ]Coastal Research and Education Center, Clemson University, 2700 Savannah Hwy, Charleston, SC 29414
                [8 ]Department of Plant Pests and Diseases, Faculty of Agriculture, Bogor Agricultural University, Bogor 16144, Indonesia
                [9 ]CABI, Bakeham Lane, Egham, Surrey TW20 9TY, UK
                [10 ]Agroecology/IPM program, DCE Crop Systems Intensification and Climate Change (CSI-CC), International Potato Center, Av. La Molina 1895, Lima 12, Peru
                [11 ]School of Sciences, Saint Francis University, P.O. Box 600, Loretto, PA 15940
                [12 ]International Potato Center, Global Crop Diversity Trust, Present address: Sonnenhalde 21, 70794 Filderstadt, Germany
                [13 ]Department of Evolutionary and Environmental Biology, University of Haifa, Haifa 31905, Israel
                [14 ]Pampanga State Agricultural University, Magalang, Pampanga 2010, Philippines
                [15 ]Department of Invertebrate Pests and Weeds, Division of Biotechnology and Plant Health, NIBIO-Norwegian Institute of Bioeconomy Research, Høgskolevegen 7, 1430 Ås, Norway
                [16 ]School of Environmental Sciences, University of Guelph, Guelph, ON, Canada N1G 2W1
                [17 ]Department of Biology, Mugla Siki Kocman University, 48170 Kotekli, Mugla, Turkey
                [18 ]State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beichen West-Road 1, Chaoyang district, Beijing 100101, PR China,
                [19 ]Crop Protection Research Centre, University of Costa Rica, San Pedro, Montes de Oca, San José, Costa Rica
                Author notes

                Subject Editor: Jessica Dohmen-Vereijssen

                [2 ]Corresponding author, e-mail: phyllisw@ 123456agri.gov.il
                Article
                iew121
                10.1093/jisesa/iew121
                5388319
                968cf14b-0618-43fb-bd2a-03877de5c706
                © The Authors 2017. Published by Oxford University Press on behalf of Entomological Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 August 2016
                : 1 December 2016
                Page count
                Pages: 27
                Categories
                Forum

                Entomology
                invasive species,biodiversity,management,parasitoids,climate model
                Entomology
                invasive species, biodiversity, management, parasitoids, climate model

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