20 research outputs found
Fig 1 -
Dynamics of woolly apple aphid populations on different parts of apples, in an apple orchard in Laiyang, Shandong Province, China, in (A) 2008 and (B) 2009.</p
Comparison of EPG parameters of woolly apple aphid <i>Eriosoma lanigerum</i> during phloem feeding on four different apple parts.
Comparison of EPG parameters of woolly apple aphid Eriosoma lanigerum during phloem feeding on four different apple parts.</p
The percentage of various waveforms’ (average duration) of per aphid (<i>Eriosoma lanigerum</i>) feeding on different parts of apple tree for eight hours.
The percentage of various waveforms’ (average duration) of per aphid (Eriosoma lanigerum) feeding on different parts of apple tree for eight hours.</p
Comparison of EPG parameters of woolly apple aphid, <i>Eriosoma lanigerum</i>, during non-phloem feeding on four parts of apple trees (var. Starkrimson).
Comparison of EPG parameters of woolly apple aphid, Eriosoma lanigerum, during non-phloem feeding on four parts of apple trees (var. Starkrimson).</p
Fig 2 -
(A) Numbers and (B) area (cm2) of aphid colonies per part on various plant parts on 15 apple varieties, in an apple orchard in Qingdao, Shandong Province, China, in June 20, 2010.</p
The daily and total (within life stage) food consumption (as mg) of <i>A</i>. <i>lucorum</i> when fed green bean pods at 25 ± 1°C, with a 16:8 h L:D photoperiod and 70 ± 5% relative humidity.
<p>The daily and total (within life stage) food consumption (as mg) of <i>A</i>. <i>lucorum</i> when fed green bean pods at 25 ± 1°C, with a 16:8 h L:D photoperiod and 70 ± 5% relative humidity.</p
Levels of Salivary Enzymes of <i>Apolygus Lucorum</i> (Hemiptera: Miridae), From 1<sup>st</sup> Instar Nymph to Adult, and Their Potential Relation to Bug Feeding
<div><p>In recent years, <i>Apolygus lucorum</i> has caused increasing damage to cotton and fruit trees in China. The salivary enzymes secreted by <i>A</i>. <i>lucorum</i> when sucking on host plants induce a series of biochemical reactions in plants, and the pre-oral digestion benefits the bug feeding. In this study, the food intake of <i>A</i>. <i>lucorum</i> from 1<sup>st</sup> instar nymphs to adults was measured, and the corresponding salivary activity of pectinase, amylase, cellulase, protease, polyphenol oxidase and peroxidase was determined. Daily food intake varied with developmental stage, peaking in 3<sup>rd</sup> and 4<sup>th</sup> instar nymphs. Pectinase, amylase, cellulase and protease were detected in both nymphal and adult saliva of <i>A</i>. <i>lucorum</i>, while neither polyphenol oxidase nor peroxidase was detected. Protease activity varied with food intake peaking at the 3<sup>rd</sup>-4<sup>th</sup> instar, and then slightly decreasing at the 5<sup>th</sup> instar. Levels of pectinase, amylase and cellulase increased significantly with the daily feeding level until the 3<sup>rd</sup> instar, corresponding with increasing damage to host plants. The activity of both cellulase and protease had a significant linear relationship with the average daily food intake. The increasing activity of enzymes in saliva explain stage-specific impacts of <i>A</i>. <i>lucorum</i> on the host plants, and suggest that optimal management of <i>A</i>. <i>lucorum</i> would be confined to its control threshold prior to the peak of daily feeding in the 3<sup>rd</sup> instar.</p></div
Adapted finite difference schemes advection-reaction-diffusion problems generating periodic wavefronts
The talk is focused on the numerical integration of advection-reaction-diffusion problems by finite difference schemes adapted to problem. In other terms, the numerical scheme, exploiting the a-priori knowledge of the qualitative behaviour of the solution, gains ad- vantages in terms of efficiency and accuracy with respect to classic schemes already known in literature. The adaptation is here carried out through the so-called trigonometrical fitting technique for the discretization in space, giving rise to a system of ODEs whose vector field contains both stiff and non-stiff terms. Due to this mixed nature of the vector field, an Implicit-Explicit (IMEX) method is here employed for the integration in time, based on the first order forward-backward Euler method. The coefficients of the method introduced rely on unknown parameters which have to be properly estimated: such an estimate is performed by minimizing the leading term of the local truncation error in an efficient way. The effectiveness of this problem-oriented approach is shown through a rigorous theoretical analysis and some numerical experiments.
References
[1] R. D’Ambrosio, M. Moccaldi and B. Paternoster, Adapted numerical schemes for advection-reaction-diffusion problems generating periodic wavefronts, Comp. Math. Appl. (2017).
[2] A.J. Perumpanani, J.A. Sherratt, P.K. Maini, Phase differences in reac- tion–diffusion–advection systems and applications to morphogenesis, J. Appl. Math. 55, 19-33 (1995)
The number of pupae, progeny produced, emergence rate, sex ratio (as %F)and relative compatibility of backcross.
The number of pupae, progeny produced, emergence rate, sex ratio (as %F)and relative compatibility of backcross.</p
The base content, AT skewness and GC skewness of the two <i>Aphelinus mali</i> clades compared to other Hymenoptera.
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