How to better predict long-term benefits and risks in weed biocontrol: an evolutionary perspective
Tài liệu tham khảo
Müller-Schärer, 2008, Classical biological control: exploiting enemy escape to manage plant invasions, Biol Invasions, 10, 859, 10.1007/s10530-008-9238-x
Schwarzländer, 2018, Biological control of weeds: an analysis of introductions, rates of establishment and estimates of success, worldwide, BioControl, 63, 319, 10.1007/s10526-018-9890-8
Hinz, 2019, How safe is weed biological control? A global review of direct nontarget attack, Q Rev Biol, 94, 1, 10.1086/702340
McEvoy, 2012, Evolving while invading: rapid adaptive evolution in juvenile development time for a biological control organism colonizing a high-elevation environment, Evol App, 5, 524, 10.1111/j.1752-4571.2012.00278.x
Heimpel, 2017
Helliwell, 2018, Rapid establishment of a flowering cline in Medicago polymorpha after invasion of North America, Mol Ecol, 27, 4758, 10.1111/mec.14898
Sotka, 2018, Combining niche shift and population genetic analyses predicts rapid phenotypic evolution during invasion, Evol App, 11, 781, 10.1111/eva.12592
van Boheemen, 2019, Rapid and repeated local adaptation to climate in an invasive plant, New Phytol, 222, 614, 10.1111/nph.15564
Winston, 2014
Stastny, 2017, Evidence for rapid evolutionary change in an invasive plant in response to biological control, J Evol Biol, 30, 1042, 10.1111/jeb.13078
Fukano, 2012, Changes in defense of an alien plant Ambrosia artemisiifolia before and after the invasion of a native specialist enemy Ophraella communa, PLoS One, 7, 10.1371/annotation/868d00f2-375e-421f-8435-0e628c0567bd
Sun, 2019, Rapid evolution of invasive traits facilitates the invasion of common ragweed, Ambrosia artemisiifolia, J Ecol, 107, 2673, 10.1111/1365-2745.13198
Wright, 2018, Evolution of biological control agents following introduction to new environments, BioControl, 63, 105, 10.1007/s10526-017-9830-z
Szűcs, 2019, The implications of rapid eco-evolutionary processes for biological control - a review, Entomol Exp Appl, 167, 598, 10.1111/eea.12807
Griffith, 2019, Thermal plasticity and microevolution enhance establishment success and persistence of a water hyacinth biological control agent, Entomol Exp Appl, 167, 616, 10.1111/eea.12814
Bean, 2012, Evolution of critical day length for diapause induction enables range expansion of Diorhabda carinulata, a biological control agent against tamarisk (Tamarix spp.), Evol App, 5, 511, 10.1111/j.1752-4571.2012.00262.x
Fukano, 2016, Contemporary evolution of host plant range expansion in an introduced herbivorous beetle Ophraella communa, J Evol Biol, 29, 757, 10.1111/jeb.12824
Szűcs, 2012, Post-introduction evolution in the biological control agent Longitarsus jacobaeae (Coleoptera: Chrysomelidae), Evol App, 5, 858, 10.1111/j.1752-4571.2012.00264.x
Mathenge, 2010, Hybridization between Dactylopius tomentosus (Hemiptera: Dactylopiidae) biotypes and its effects on host specificity, Bull Entomol Res, 100, 331, 10.1017/S0007485309990344
Schaffner, 2001, Host range testing of insects for biological weed control: how can it be better interpreted? Data on the host range of biocontrol candidates are particularly relevant in assessing potential detrimental effects to nontarget organisms, Bioscience, 51, 951, 10.1641/0006-3568(2001)051[0951:HRTOIF]2.0.CO;2
Le Hesran, 2019, Next generation biological control–an introduction, Entomol Exp Appl, 167, 579, 10.1111/eea.12805
Lirakis, 2019, Does experimental evolution produce better biological control agents? A critical review of the evidence, Entomol Exp Appl, 167, 584, 10.1111/eea.12815
Grevstad, 1999, Factors influencing the chance of population establishment: implications for release strategies in biocontrol, Ecol Appl, 9, 1439, 10.1890/1051-0761(1999)009[1439:FITCOP]2.0.CO;2
Webber, 2015, Opinion: is CRISPR-based gene drive a biocontrol silver bullet or global conservation threat?, Proc Natl Acad Sci U S A, 112, 10565, 10.1073/pnas.1514258112
Kawecki, 2012, Experimental evolution, Trends Ecol Evol, 27, 547, 10.1016/j.tree.2012.06.001
Barrick, 2013, Genome dynamics during experimental evolution, Nat Rev Genet, 14, 827, 10.1038/nrg3564
Cooper, 2018, Experimental evolution as a high-throughput screen for genetic adaptations, Msphere, 3, e00121, 10.1128/mSphere.00121-18
Schlötterer, 2015, Combining experimental evolution with next-generation sequencing: a powerful tool to study adaptation from standing genetic variation, Heredity, 114, 431, 10.1038/hdy.2014.86
Messina, 2017, Evolution of host acceptance and its reversibility in a seed beetle, Ecol Entomol, 42, 42, 10.1111/een.12352
Price, 2017, Warp-speed adaptation to novel hosts after 300 generations of enforced dietary specialisation in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae), Eur J Entomol, 114, 257, 10.14411/eje.2017.031
Rêgo, 2019, Dynamics of genomic change during evolutionary rescue in the seed beetle Callosobruchus maculatus, Mol Ecol, 28, 2136, 10.1111/mec.15085
Gompert, 2016, Genomic evidence that resource-based trade-offs limit host-range expansion in a seed beetle, Evolution, 70, 1249, 10.1111/evo.12933
Hopper, 1993, Management of genetics of biological-control introductions, Annu Rev Entomol, 38, 27, 10.1146/annurev.en.38.010193.000331
DeBach, 1991
Szűcs, 2014, The roles of demography and genetics in the early stages of colonization, Proc R Soc B Biol Sci, 281
TAG-BCAW-Manual, 2016
Müller-Schärer, 2018, Cross-fertilizing weed science and plant invasion science to improve efficient management: a European challenge, Basic Appl Ecol, 33, 1, 10.1016/j.baae.2018.08.003
Zhou, 2014, Control of the invasive weed Ambrosia artemisiifolia with Ophraella communa and Epiblema strenuana, Biocontrol Sci Technol, 24, 950, 10.1080/09583157.2014.897305
Müller‐Schärer, 2014, Ophraella communa, the ragweed leaf beetle, has successfully landed in Europe: fortunate coincidence or threat?, Weed Res, 54, 109, 10.1111/wre.12072
Futuyma, 1995, Genetic constraints on macroevolution: the evolution of host affiliation in the leaf beetle genus Ophraella, Evolution, 49, 797, 10.1111/j.1558-5646.1995.tb02316.x
Futuyma, 1993, Genetic constraints and the phylogeny of insect-plant associations: responses of Ophraella communa (Coleoptera: Chrysomelidae) to host plants of its congeners, Evolution, 47, 888, 10.1111/j.1558-5646.1993.tb01242.x
Osenberg, 1994, Detection of environmental impacts: natural variability, effect size, and power analysis, Ecol Appl, 4, 16, 10.2307/1942111
de Villemereuil, 2016, Common garden experiments in the genomic era: new perspectives and opportunities, Heredity, 116, 249, 10.1038/hdy.2015.93
Long, 2015, Elucidating the molecular architecture of adaptation via evolve and resequence experiments, Nat Rev Genet, 16, 567, 10.1038/nrg3937
Nuzhdin, 2013, Promises and limitations of hitchhiking mapping, Curr Opin Genet Dev, 23, 694, 10.1016/j.gde.2013.10.002
Dawson, 2014, Natural experiments and meta-analyses in comparative phylogeography, J Biogeogr, 41, 52, 10.1111/jbi.12190
Hoffmann, 2011, Climate change and evolutionary adaptation, Nature, 470, 479, 10.1038/nature09670
Carroll, 2005, And the beak shall inherit–evolution in response to invasion, Ecol Lett, 8, 944, 10.1111/j.1461-0248.2005.00800.x
Dingle, 2009, Influence of genetic architecture on contemporary local evolution in the soapberry bug, Jadera haematoloma: artificial selection on beak length, J Evol Biol, 22, 2031, 10.1111/j.1420-9101.2009.01819.x
Kellermann, 2019, Terrestrial insects and climate change: adaptive responses in key traits, Physiol Entomol, 44, 99, 10.1111/phen.12282
Müller-Schärer, 2019, Predicting benefits and risks of biological control of the invasive common ragweed in Europe: from ecological to evolutionary studies, 151
Hufbauer, 2002, Evidence for nonadaptive evolution in parasitoid virulence following a biological control introduction, Ecol Appl, 12, 66, 10.1890/1051-0761(2002)012[0066:EFNEIP]2.0.CO;2
Grandgirard, 2008, Engineering an invasion: classical biological control of the glassy-winged sharpshooter, Homalodisca vitripennis, by the egg parasitoid Gonatocerus ashmeadi in Tahiti and Moorea, French Polynesia, Biol Invasions, 10, 135, 10.1007/s10530-007-9116-y
Grevstad, 2015, The consequences of photoperiodism for organisms in new climates, Ecol Appl, 25, 1506, 10.1890/14-2071.1
