Relevant bibliographies by topics / Myzus persicae (Sulzer)

Academic literature on the topic 'Myzus persicae (Sulzer)'

Author: Grafiati
Published: 10 December 2022
Last updated: 19 February 2023

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Journal articles on the topic "Myzus persicae (Sulzer)"

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Kumar, Surjeet, and Omkar Gavkare. "Lifetable of Myzus Persicae (Sulzer) on capsicum annuum." Indian Journal of Entomology 79, no. 1 (2017): 115. http://dx.doi.org/10.5958/0974-8172.2017.00024.4.

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Xiuyun Zhao, Jianhong Yao,, Huaxiong Qi, Bingliang Wan, Fei Chen, Xiaofen Sun, Shanqian Yu, and Kexuan Tang. "Transgenic tobacco expressing an Arisaema heterophyllum agglutinin gene displays enhanced resistance to aphids." Canadian Journal of Plant Science 84, no. 3 (July 1, 2004): 785–90. http://dx.doi.org/10.4141/p03-036.

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Tobacco leaf discs were transformed with a plasmid, pBIAHA, containing the selectable marker neomycin phosphotransferase gene (nptII) and an Arisaema heterophyllum agglutinin gene (aha) via Agrobacterium tumefaciens-mediated transformation. Thirty-two independent transgenic tobacco plants were regenerated. PCR and Southern blot analyses confirmed that multiple copies of the aha gene had integrated into the plant genome. Northern blot analysis revealed that the aha gene was expressed at various levels in the transgenic plants. Insect bioassay test showed that transgenic plants expressing multiple copies of the aha gene reduced the rate of population increase of the peach potato aphid (Myzus persicae Sulzer). This is the first report that transgenic tobacco plants expressing the aha gene display enhanced resistance to aphids. Key words: Insect bioassay, Arisaema heterophyllum agglutinin, transformation, transgenic tobacco, peach potato aphid (Myzus persicae Sulzer)
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Vucetic, Andja, Olivera Petrovic-Obradovic, and Lj Z. Stanisavljevic. "The morphological variation of Myzus persicae (Hemiptera: Aphididae) from peach and tobacco in Serbia and Montenegro." Archives of Biological Sciences 62, no. 3 (2010): 767–74. http://dx.doi.org/10.2298/abs1003767v.

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Multivariate morphometric analysis was used to compare nine characteristics of 47 populations of Myzus persicae (Sulzer) originating from two host-plants, peach and tobacco, from 13 localities in 2004 and 34 localities in 2005, in Serbia and Montenegro. Multivariant discriminant analysis showed there to be a distinct discrimination between the populations from the peach and tobacco host-plants. The most important discrimination characteristics are the ultimate rostral segment length and processes terminalis length, which are greater in the aphids from tobacco than in those from peach. This is the first indication that in this part of Europe there are two subspecies: M. persicae (Sulzer) and M. persicae nicotianae Blackman. .
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Boiteau, Gilles, and D. T. Lowery. "COMPARISON OF A YELLOW FORM OF THE GREEN PEACH APHID, MYZUS PERSICAE (SULZER), AND A GREEN FORM OF THE TOBACCO APHID, MYZUS NICOTIANAE BLACKMAN, COEXISTING ON GREENHOUSE POTATO IN NEW BRUNSWICK." Canadian Entomologist 121, no. 12 (December 1989): 1029–35. http://dx.doi.org/10.4039/ent1211029-12.

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AbstractA dark green aphid was isolated from a greenhouse colony of green peach aphid, Myzus persicae (Sulzer), in Fredericton, N.B. The green aphid was shown to conform taxonomically and biologically to the recently named species Myzus nicotianae Blackman, except for its rare production of alatae. It is reported for the first time on greenhouse-grown potato where its population development is similar to that of the yellow holocyclic M. persicae from the same colony. The vector efficiency of the green and yellow aphids for potato virus Y0 is similar. The yellow aphid tends to be more susceptible to insecticides than the green aphid. Myzus nicotianae was not found in aerial aphid samples taken in New Brunswick in 1967 and 1987.
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Hales, D. F., P. W. Wellings, and R. A. Parkes. "Investment in Gynoparae and Males by Myzus persicae (Sulzer)." Functional Ecology 3, no. 6 (1989): 727. http://dx.doi.org/10.2307/2389505.

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BLACKMAN, R. L., and H. TAKADA. "A naturally occurring chromosomal translocation in Myzus persicae (Sulzer)." Journal of Entomology Series A, General Entomology 50, no. 3 (April 2, 2009): 147–56. http://dx.doi.org/10.1111/j.1365-3032.1976.tb00129.x.

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Ortiz, Menandro S., Cecilia R. Escajadillo, and Verónica E. Rubin de Celis. "Aphididae (Hemiptera) procedentes del valle de Ica-Perú." Biotempo 7 (September 4, 2017): 28–38. http://dx.doi.org/10.31381/biotempo.v7i0.870.

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Se reportan las siguientes especies procedentes del valle de Ica: Aphis citricola Van der Goot, Aphis craccivora Koch, Aphis gossypii Glover, Toxoptera aurantii (Boyer de Fonscolombe), Toxoptera citricidus (Kirkaldy), Macrosiphum rosae (Linnaeus), Myzus persicae (Sulzer), Hyalopterus pruni (Geoffroy), Rhopalosiphum maidis (Fitch), Rhopalosiphum rufiabdominalis (Sasaki), Uroleucon (Lambersius) erigeronensis (Thomas) y Wahlgreniella nervata (Gillette).
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Ortego, Jaime. "IMPORTANCIA DE LOS HOSPEDEROS PRIMARIOS DE Myzus persicae Sulzer EN LA EPIDEMIOLOGÍA DEL PVY." Revista Latinoamericana de la Papa 5, no. 1 (April 30, 2016): 64–76. http://dx.doi.org/10.37066/ralap.v5i1.59.

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Se investigó el rol de los hospederos primarios de M. persicae, principal vector de PVY, en la epidemiología de este virus en Malargüe, Mendoza, Argentina, en un área protegida para la producción de tubérculos semilla de papa. En el ciclo 1989- 1990, se realizó un relevamiento de este áfido sobre posibles hospederos primarios y secundarios. Se estudió el ciclo biológico de M. percicae en el área de estudio. Se efectuó un análisis morfométrico de individuos alados de esta especie, capturados en trampas amarillas de agua, lo que permitió determinar la proporción de formas holocíclicas y anholocíclicas presentes. Solamente Prunus percica y P. pissardii resultaron colonizados por M. persicae, constatándose además, que esta especie puede invernar también en forma partenogenética sobre hospederos secundarios. El análisis morfométrico indicó que las formas holocíclicas pueden representar entre el 50 y 100% de los individuos alados que visitan cultivos de papa al comienzo del ciclo, cuando las plantas son más sensibles al PVY. Esto indica que la relevancia de hospederos primarios especialmente durazneros (P. persica), en a la dispersión temprana del virus.Aceptado para publicación: abril 2, 1994
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Blackman, R. L. "Morphological discrimination of a tobacco-feeding form from Myzus persicae (Sulzer) (Hemiptera: Aphididae), and a key to New World Myzus (Nectarosiphon) species." Bulletin of Entomological Research 77, no. 4 (December 1987): 713–30. http://dx.doi.org/10.1017/s0007485300012219.

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AbstractMultivariate techniques, principally the method of canonical variates, were used to investigate morphological variation within and between populations of the group of Myzus persicae (Sulzer) from North and South America, Europe, Africa and Asia. The scores on the first canonical variate of samples from tobacco in North America, the Mediterranean region, the Middle East, Africa and Sri Lanka all grouped consistently when compared with samples from other host-plants, even after aphids from tobacco had been reared for up to seven years on a non-tobacco host. Thus there is a widely-distributed tobacco-adapted form, closely related to M. persicae but with its own characteristic morphology. Morphological discriminants are given for the recognition of apterous and alate viviparae of this tobacco form, which is given the name M. nicotianae sp. n. Both M. persicae and M. nicotianae have 2n = 12, and both are frequently heterozygous for apparently the same autosomal translocation, which they must have acquired independently. M. nicotianae is presumably isolated from M. persicae by being permanently parthenogenetic. In Japan and Central Asia, however, aphids of the M. persicae group on tobacco can produce sexual morphs; the taxonomic status of these latter populations is still unclear. Multivariate comparison of European and North American populations of dark green aphids of the M. persicae group with 13 or 14 chromosomes in somatic cell nuclei instead of the normal 12, led to the conclusion that these all belong to one morphologically variable taxon, M. antirrhinii (Macchiati). Keys are provided to the apterous and alate virginoparae of the species of the M. persicae group in America.
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Jung, Ji Young, Hyung Chul Lee, and Jae-Kyung Yang. "Insecticidal Activity of Coptis chinensis Extract Against Myzus persicae (Sulzer)." Journal of the Korean Wood Science and Technology 43, no. 2 (March 25, 2015): 274–85. http://dx.doi.org/10.5658/wood.2015.43.2.274.

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Dissertations / Theses on the topic "Myzus persicae (Sulzer)"

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Little, E. J. "Insecticide resistance£t in the aphid Myzus persicae (Sulzer)." Thesis, University of Leeds, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235363.

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Saljoqu, Ahmad-Ur-Rahman. "Integrated management of potato aphid, Myzus persicae (Sulzer) in Pakistan." Thesis, University of Reading, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284450.

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Hag, Ahmed Saif Eldin Mohamed Kheir. "Biological control of glasshouse Myzus persicae (Sulzer) using Aphidius matricariae Haliday." Thesis, Imperial College London, 1990. http://hdl.handle.net/10044/1/46324.

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Pegadaraju, Venkatramana. "Molecular insights into arabidopsis response to Myzus persicae sulzer (green peach aphid)." Diss., Manhattan, Kan. : Kansas State University, 2005. http://hdl.handle.net/2097/129.

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Clough, Martin S. "Cold hardiness and overwintering of the peach-potato aphid Myzus persicae (Sulzer)." Thesis, University of Leeds, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305665.

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Hinga, Clark D. "Genetic analysis of resistance to Myzus persicae (Sulzer) in Nicotiana tabacum L." Thesis, Virginia Tech, 1985. http://hdl.handle.net/10919/41552.

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Field experiments with the green peach aphid on tobacco were conducted at Blackstone, Virginia in 1983 and 1984. The objectives were to: 1) confirm and identify source materials resistant to the green peach aphid; 2) study the inheritance of aphid resistance; 3) verify heritability of resistant genotypes through F2 and advanced generation testing and 4) investigate the nature of the resistance.

Results showed green peach aphid resistance in Tobacco Introductions 1462, 1118, 1112, 1024, breeding line 1-35 and cultivar NC 745. Inheritance studies showed that the resistance is a recessive trait controlled by three separate, non-linked loci; such that a homozygous recessive at any one locus will condition for the resistance reaction. Among the source materials, one locus conditioned the resistance shown by TI 1118, TI 1112 and breeding line I-35. A second independent locus conditioned the found in TI 1024 and a third independent locus conditioned the resistance observed in NC 745. Tobacco Introduction 1462 possessed alleles for resistance at both the second and third loci.

Small aphid cages were of questionable value for studying the resistance reaction. Higher leaf temperatures were noted for the caged leaf surfaces and may be responsible for the unreliable results.

Evaluation of F2, F3, F5, F5 populations developed from resistant x susceptible crosses indicated that aphid resistance is a heritable trait and is not closely linked to adverse agronomic quality characteristics.


Master of Science
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Marie, Joan. "Intraclonal Morphological Plasticity within the Myzus persicae (Sulzer) Complex Related to Host Plant and Temperature." Thesis, Virginia Tech, 2004. http://hdl.handle.net/10919/33305.

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Blackman (1987) used life cycle and morphology to separate Myzus nicotianae Blackman, a tobacco-feeding species of aphid, from Myzus persicae (Sulzer). In the present study, the first objective was to investigate the influence of temperature and host plant on the morphology of M. nicotianae and M. persicae. The second objective was to assess Blackman¡¦s 1987 key to Myzus for separating tobacco and non-tobacco originating morphs under different environmental conditions. Four host plants were used: tobacco, turnip, pepper, and okra, and three temperatures, 15â aC, 20â aC, and 25â aC. The intraclonal plasticity of two tobacco collected morphs and one turnip collected morph was investigated in relation to these combinations of host and temperature in a 4 x 3 x 3 factorial experimental design. Fifth generation mature apterous aphids were mounted on slides and 10 different morphological structures utilized in morphometric analysis were measured. Data support a morphologically distinct, host-adapted tobacco race but not a separate tobacco-feeding species of M. persicae. The key developed by Blackman (1987) did not discriminate between the tobacco and non-tobacco originating clones but the canonical variates generated from the analysis successfully separated the tobacco and non-tobacco groups. Other studies have used many different clones to investigate the possible distinctions between M. persicae and M. nicotianae; the objective here was to see how much morphological perturbation may be induced within a clone by rearing at different temperatures and on different host plants. Temperature and host plant had substantial influences on the morphology of these aphids. The physiological interactions of temperature-host plant-aphid morphology are very complex yet controlling only for temperature and host plant was sufficient to group specimens according to these independent variables with remarkable accuracy using the linear discriminant functions generated with these data. Percent of aphids in which rearing temperature was correctly identified using linear discriminant functions generated for temperature classes was 87%, 63%, and 64% for 15â aC, 20â aC, and 25â aC, respectively. Random designations would be 33%. Correct identification of host plant was 65%, 45%, 47%, and 48% successful for tobacco, turnip, pepper, and okra, respectively. Random designations for host plant would be 25%. Canonical variates produced clusters by host, temperature, morph, and combinations of these independent variables with varying degrees of discreteness. CV1 by CV2 for host plants gave a very distinct cluster for tobacco and also separate groupings for aphids reared on turnip and pepper. Aphids from the host plant okra were scattered quite widely across the CV1 by CV2 graph. CV1 by CV2 for temperature conditions showed a tight cluster for aphids from 15â aC and still distinct though less closely grouped clusters for both 20â aC and 25â aC rearing temperatures. CV1 by CV2 for the three morphs gave substantial overlap for the two tobacco originating morphs and a more separate cluster for the morph originally collected from turnip.
Master of Science
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Srigiriraju, Lakshmipathi. "Quantification of insecticide resistance in the tobacco-adapted form of the green peach aphid, Myzus persicae (Sulzer)(Hemiptera: Aphididae)." Diss., Virginia Tech, 2008. http://hdl.handle.net/10919/27549.

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The tobacco-adapted form of the green peach aphid, Myzus persicae (Sulzer), is one of the most important insect pests of tobacco in the United States and around the world. Insecticides play a major role in controlling the aphid on tobacco because natural enemies usually fail to maintain its populations below damaging levels. The aphid has a history of developing resistance to many insecticides. Therefore, baseline information on the aphidâ s susceptibility to imidacloprid and other insecticides is critical for developing future resistant management programs to minimize losses attributed to the aphid. Studies were conducted on colonies of the tobacco-adapted form of the green peach aphid collected from nine states in the eastern United States in 2004-2007. The susceptibility of 151 colonies to imidacloprid was determined in serial leaf-dip bioassays. When combined over the four years, 18, 14, and 4% of the colonies had 10- to 20-fold, 20- to 30-fold, and 30- to 90-fold resistance ratios, respectively, suggesting that high levels of resistance to imidacloprid are present in field populations of the aphid. A colony collected near Clayton, NC had the highest LC50 value (31 ppm) combined over six tests and three years, but the average resistance ratios for the first three runs was over 130-fold (48 ppm). Geographic location had little effect on susceptibility to imidacloprid. Aphid colonies (136) including red, green, and orange color morphs were screened for total esterase activity using microplate assay with 1-Naphthyl acetate as the substrate. The green morphs generally had lower esterase levels than the red and orange morphs. All orange morphs had among the highest esterase activities. Esterase activities of red and green morphs were positively correlated with LC50 values as determined by leaf-dip bioassays for acephate and methomyl. All 25 colonies tested for esterase gene amplification had either E4 or FE4 gene amplification. The amplification of both E4 and FE4 seen as an 865-bp band characteristic of the FE4 gene and an additional 381-bp band characteristic of a deleted upstream region of the E4 gene occurred in all (4) orange morphs and one (1 of 9) green morph. Target-site insensitivity of acetylcholinesterase (AChE), as modified AChE resistance (MACE) was assessed in 65 colonies of field-collected tobacco-adapted forms of M. persicae. Eight colonies over a range of AChE activity were selected to study inhibition of AChE in the presence of two carbamate insecticides, methomyl and pirimicarb. IC50 values for methomyl ranged from 0.35 to 2.4 μM while six of eight colonies had lower values with a range of 0.16 to 0.30 μM for pirimicarb. Two colonies that were inhibited by methomyl had very high IC50 values of 40.4 and 98.6 μM for pirimicarb. Such insensitivity may be due to mutations in the ace2 gene, but this needs to be confirmed by genetic and molecular analysis. Glutathione S- transferases (GSTs), isoenzymes that are involved in the metabolism and detoxification of many xenobiotic compounds were quantified for 100 colonies by CDNB conjugation. There was a wide range of GST activity for the red (8 to 343 pmol/min/mg protein) and green (15.3 to 330 pmol/min mg protein) morphs, but all six orange morphs collected in 2007 had a narrower range (160 to 211 pmol/min/mg protein). About 45% of the red morphs had GST activity from 200-300 pmol/min/mg of protein, while 53% of the green morphs had a range of 100-200 pmol/min/mg protein. The influence of temperature-mediated synergisms on the toxicity of insecticides in red and green color morphs of the tobacco-adapted from of M. persicae were evaluated using leaf-dip bioassay procedures in laboratory incubators. Post-exposure temperatures of 15, 20, and 25oC were evaluated for four classes of insecticides, acephate, imidacloprid, lambda-cyhalothrin, and methomyl. The temperature change from 15 to 20oC caused almost a 3-fold increase in toxicity to the red and green color morphs for methomyl, acephate, and imidacloprid. In contrast, the toxicity of lambda-cyhalothrin decreased as the temperature increased, showing a negative temperature coefficient. Bioassay experiments conducted with the red morph for indirect estimates of imidacloprid concentrations in flue-cured tobacco showed that leaf position, imidacloprid rate and time after application affected the concentration of the toxicant in the leaf. The differences in aphid mortality between the lower and upper leaf positions indicate that the concentration of imidacloprid and its metabolites were unevenly distributed with the lowest mortality for aphids feeding on the younger, upper leaves and the highest for those feeding on the older, lower leaves. In field experiments, higher aphid populations occurred on tobacco treated with imidacloprid less than the field recommended rate of 41.4 ml/1,000 plants. The development of aphid populations in the field was consistent with the laboratory bioassays. Field trials were conducted to evaluate the performance of various insecticides currently registered for aphid control on tobacco. Imidacloprid applied as a tray drench treatment and acephate as foliar sprays were the most effective treatments. Moderate declines in control with imidacloprid were observed at 75-87 d after transplanting in 2006 and 2007. Aldicarb gave good to excellent control in one of three years, but only fair to poor control in the other two years. Methomyl and lambda-cyhalothrin gave good control in all three years except the residual was shorter. The poor performance of aldicarb in the two years may have been related to the presence of E4 or FE4 resistance in the naturally occurring TGPA in the experimental plots.
Ph. D.
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O'Doherty, Rose. "Studies on the cold hardiness of the peach-potato aphid Myzus persicae (Sulzer)." Thesis, University of Leeds, 1985. http://etheses.whiterose.ac.uk/4413/.

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A system incorporating a prototype automatic thermoelectric cooling method with computer-based recording of aphid supercooling points was developed and formed the basis of cold hardiness assessment. Under laboratory culture all developmental stages of Myzus persicae had a mean inherent supercooling potential below -20°C, with first instar nymphs the most cold hardy. When maintained at 5°C, younger instars demonstrated acclimation ability unlike adult aphids, and in an insecticide resistant strain, adults lost cold hardiness. When in contact with surface moisture, the majority of aphids did not experience inoculative nucleation. Sexual morphs of M. persicae possessed supercooling ability comparable with laboratory maintained parthenogenetic morphs; eggs supercooled to below -30°C. Seasonal studies of supercooling ability demonstrated that all aphid stages were most cold hardy in summer. Younger instars showed natural acclimatisation and were cold hardy throughout the year. Overall adults lost cold hardiness as winter progressed, exhibiting bimodal supercooling point distributions in two winters, with distinct high (HG) and low (LG) groups and mean supercooling points of approximately -20°C and -10 oe respectively. Clonal differences and adult age did not account for this pattern. Following experimental starvation at 5°C, first instars of M. persicae maintained extensive supercooling potential but adults exhibited losses of cold hardiness comparable with those in natural overwintering populations, suggesting that feeding may be necessary to maintain adult cold hardiness levels during winter. Subsequent starvation experiments did not reproduce the dramatic losses of cold hardiness implying that the feeding influence was more complex than the availability of food per se. In a series of host transfer experiments the mean supercooling point of Aphis fabae adults could be shifted by over 10°C, increasing when they fed on beans and reduced when transferred back to spindle; the LG (spindle/poor supercoolers) to HG (bean/good supercoolers) shift was more difficult to achieve and suggested a nucleating agent in spindle sap. Trimethylsilyl derivatised carbohydrate extracts of M. persicae and A. fabae were analysed by capillary gas-liquid chromatography. Glucose, glycerol, fructose, mannitol, sucrose, and trehalose were detected in samples of both species, together with trace amounts of unidentified carbohydrates in M. persicae samples. Dulcitol was present in spindle-fed A. fabae only. There was no obvious correlation between carbohydrate content and supercooling ability but high total percentage body carbohydrate levels were revealed and may have a solute effect, enhancing inherent supercooling potential and dependent on carbohydrate-rich sap intake. Laboratory cultured A. fabae were capable of extensive supercooling, as were individuals collected from summer herbaceous hosts; first instars were the most cold hardy. When associated with the primary host, spindle, all aphids showed poor supercooling potential, less than -15°C; overwintering eggs were capable of supercooling to below -30°C and acclimatised in winter. Eggs and oviparae were not subject to inoculative nucleation. Preliminary experiments to relate supercooling ability to mortality at sub-zero temperatures proved inconclusive and were terminated when temperature shock and/or desiccation were thought to have induced premature mortality. The results demonstrate that the cold hardiness characteristics of M. persicae are atypical of those observed in other freezing-susceptible arthropods. It is proposed that continued feeding during mild winters maintains cold hardiness levels in adult M. persicae and this influence may provide a possible explanation for the successful anholocyclic overwintering of this aphid during such winters. Avenues of research to further investigate this proposal are suggested.
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Sauge, Marie-Hélène. "Analyse des mecanismes de la resistance du pecher prunus persica (l. ) batsch au puceron vert myzus persicae (sulzer)." Paris 6, 1999. http://www.theses.fr/1999PA066458.

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L'expression de la resistance au puceron vert myzus persicae (sulzer) a ete etudiee chez quatre varietes de pecher (prunus persica (l. ) batsch et chez le clone p1908 de l'espece prunus davidiana (carr. ) franch. Chez rubira et weeping flower peach, la resistance agit par antixenose ; elle a vraisemblablement pour origine la presence de substances phloemiennes a forte activite antiappetante ou phagorepulsive. Chez rubira, les piqures du puceron induisent des reactions de defense, qui semblent associees a des signaux que le puceron detecte dans le mesophylle et dans les faisceaux vasculaires. Chez summergrand, malo konare et p1908, la resistance agit par antibiose. Chez summergrand et malo konare, l'action depressive de la resistance sur les stades larvaires est plus marquee que chez p1908 ; les facteurs de resistance, localises dans les tissus vasculaires et dans les tubes cribles, restreignent l'activite d'ingestion de seve. Chez p1908, la fonction reproductrice du puceron est fortement affectee : un mecanisme physiologique destine a restreindre l'ecoulement de seve dans les tubes cribles est probablement responsable de la resistance. L'analyse phenotypique et genotypique de la descendance hybride summergrand p1908 a permis de caracteriser les facteurs genetiques impliques dans la resistance. Chez p1908, un qtl de resistance majeur est associe a un mecanisme de defense phloemien conduisant a la reduction de l'ingestion de seve elaboree. Un autre qtl a effet mineur gouverne l'expression de facteurs de resistance localises dans le mesophylle et dans le parenchyme vasculaire. Le qtl de resistance detecte chez summergrand est associe a des facteurs de resistance pre-phloemiens et phloemiens, qui retardent l'apparition de l'ingestion et perturbent l'installation des styles du puceron dans les tubes cribles. Le caractere complementaire des resistances conferees par l'ensemble de ces genotypes permet d'envisager la construction d'une resistance durable a m. Persicae chez le pecher.
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Books on the topic "Myzus persicae (Sulzer)"

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Birt, Andrew Guy. The dynamics of over-wintering myzus persicae (sulzer.) populations. Birmingham: University of Birmingham, 2002.

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Book chapters on the topic "Myzus persicae (Sulzer)"

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Peck, Stewart B., Carol C. Mapes, Netta Dorchin, John B. Heppner, Eileen A. Buss, Gustavo Moya-Raygoza, Marjorie A. Hoy, et al. "Green Peach Aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae)." In Encyclopedia of Entomology, 1727–30. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_1189.

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Melia, A. "Seasonal evolution of Myzus persicae (Sulz.) (Homoptera, Aphidoidea) with relation to citrus fruit trees." In Integrated Pest Control in Citrus-Groves, 77–88. London: CRC Press, 2021. http://dx.doi.org/10.1201/9781003079279-17.

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MacRae, Ian, Matthew Carroll, and Min Zhu. "Site-Specific Management of Green Peach Aphid, Myzus persicae (Sulzer)." In GIS Applications in Agriculture, 167–89. CRC Press, 2011. http://dx.doi.org/10.1201/b10597-9.

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Mdellel, Lassaad, Rihem Adouani, and Monia Ben Halima Kamel. "Aphid on Almond and Peach in Tunisia: Species, Bioecology, Natural Enemies and Control Methods." In Fruit Industry [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.103966.

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Aphids are among the most obnoxious pests of almond and peach in Tunisia. Accurate control of these insect pests requires the determination of their major species as well as the thorough understanding of the biology and identification of their major natural enemies. The scope of this chapter is to identify the main aphid species infesting almond and peach in Tunisia, to describe their biology, to determine their natural enemies and to study their efficiency as biological agents. A field survey was carried out during 2007–2016 period at Almond and Peach orchards in Tunisia. Results demonstrated the presence of Hyalopterus pruni Geoffroy, Hyalopterus amygdali Blanchard, Brachycaudus amygdalinus Schouteden, Myzus persicae Sulzer, Brachycaudus schzartwi Borner and Pterochloroides persicae Cholodkovsky. Biological study of recorded species demonstrated the presence of holocyclic and anholocyclic life cycle depending on host trees and aphid species. For predators, four families (Coccinellidae, Syrphidae, Chrysopidae, Cecidomyiidae) and one parasitoid and two entomopathogenic fungi species were identified. For control of Pterochloroides persicae, results showed that Pauesia antennata Mukergi was more efficacy than Coccinella algerica Kovar. This parasitoid should be reared and used in future integrated pest management program in almond and peach orchard in Tunisia.
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Bues, R., J. F. Toubon, and H. S. Poitout. "Development of a control programme against the aphids (Macrosiphum euphorbiae Thomas and Myzus persicae Sulzer) in processing tomato cultures in the south-east of France." In Progress on Pest Management in Field Vegetables, 209–19. CRC Press, 2020. http://dx.doi.org/10.1201/9781003079347-33.

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Andrews, M., C. Bass, M. Williamson, L. Field, A. Callaghan, and G. Moores. "A single amino acid substitution found in pirimicarb-insensitive acetylcholinesterase of the peach-potato aphid, Myzus persicae (Sulz." In Cholinergic Mechanisms, 453–54. CRC Press, 2004. http://dx.doi.org/10.3109/9780203493878-65.

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Conference papers on the topic "Myzus persicae (Sulzer)"

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Barros-Parada, Wilson. "Interactions of green peach aphid,Myzus persicae(Sulzer) (Hemiptera: Aphididae) feeding and initial infestation of oriental fruit moth,Grapholita molesta(Busck) (Lepidoptera: Tortricidae)." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.114903.

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