• Korean journal of applied entomology
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• v.55 no.3
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• pp.235-243
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• 2016

The winter cherry bug, Acanthocoris sordidus (Thunberg), is an insect pest hat damages plants from Solanaceae and Convolvulaceae. The developmental period from egg to adult averages 76 days at $25^{\circ}C$. Adult egg-laying occurred irregularly via spawning, averaging 195 (up to 468) eggs per individual on the abaxial leaf surface of the host plant. Results of linear regression indicated that the lower developmental threshold temperature was $13.9^{\circ}C$ and the effective accumulated temperature was 526.3 DD. Data from a pepper field in 2015 indicated that overwintering adults first appeared during late June (daily average temperature = $25.7^{\circ}C$), reaching maximum density by early September. A choice test examining colonization preferences using a net cage and a Y-tube olfactometer revealed that females gravitated toward conspecifics (other females, males, or both), whereas males moved toward empty areas. Finally, we found that communal breeding results in a longer developmental period and higher eclosion rates than solitary breeding. Developmental periods and eclosion rates were also for colonies in a large space than for those in a small space. This outcome suggests that colonization effects on insect development are stronger in a smaller area.

• Korean journal of applied entomology
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• v.35 no.1
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• pp.38-44
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• 1996

These experiments were conducted to investigate the ecological characteristics of Amblyseius womersleyi Schica,which was biological agent in the integrated management of tea red spider mite, Tetranychus kanzawai Kishida.At four constant temperatures of 15, 20, 25, and 30$^{\circ}$C, the periods of A. womersleyi from egg to adult emergencewere 22.8, 9.6, 4.8, and 3.6 days, respectively. Developmental threshold and effectively cumulative degree-day from egg to adult emergence were 12.7"C and 61.4DD, respectively. Preoviposition periods of A.womersleyi were shorter than oviposition and postoviposition periods. The number of eggs laid per female was21.7, 28.1, 34.2, and 48.0 at the respective temperatures. The intrinsic rates of increase were estimated to be 0.064, 0.139, 0.349, and 0.402; the mean generation times were 36.0, 19.3, 8.6, and 7.7 days; the populationdoubling times were 10.8, 5.0, 2.0, and 1.7 days, respectively. A. womersleyi overwintered on green weeds, fallenleaves and in the soil surface as adult females. A. womersleyi gravid female consumed 3.0, 4.9, 15.7, and19.4 eggs of T. kanzawai per day at 15, 20, 25, and 30$^{\circ}$C, respectively. A. womersleyi protonymph consumed4.6 eggs, deutonymph 6.3 eggs, and female during oviposition consumed 19.4 eggs, and 6.8 eggs of T. kanzawaiduring postoviposition per day at 30$^{\circ}$C. at 30$^{\circ}$C.

• Korean Journal of Medicinal Crop Science
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• v.6 no.4
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• pp.328-332
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• 1998

This study was carried out to investigate the occurrence and ecological characteristics of Ostrinia furnacalis(Guenee) in Yonchon, northern part of Kyonggi province, where it is main production region of adlay in Korea. The Asian corn borer in adlay field had three generations a year. The first stage of adult activity was greatest from middle May to late June, the second from late July to middle August and the third from late August to middle September. The egg period was $3{\sim}4$ days. The longevity of adult was $7{\sim}11$ days. The days of each development stage from egg to adult were $51{\sim}61$, $33{\sim}42$ and $29{\sim}37$ days in 1st, 2nd and 3rd generations, respectively. The overwintering stage of Asian corn borer was the last instar larvae and it overwintered in the adlay stubbles.

• Korean Journal of Environmental Agriculture
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• v.21 no.1
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• pp.50-56
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• 2002

This experiment was carried out to obtain some information about overwintering, physiological and ecological characteristics of apple snails. Another purpose of this experiment was to characterize an appetite for rice plants by apple snails and to elucidate their choice of fresh green ones (vegetables, some other crops, weeds in rice fields). The freshwater snails were found with higher population at sites abundant organic compounds such as plant debris and at regions with high temperature. They also prefer calcium-rich water. This is a naturally occurring process. Apple snails were exceptionally veil-adapted to the south regions of Korea, especially Janghang, Jangseong and Haenam, even if the temperature of winter season is cold below 0$^{\circ}C$. Apple snails were not very selective in their food choice and eat almost everything available in their environment. A snail have something called a radula in its mouth for grinding up its food. A apple snail also chews on fruits and young succulent plant barks. In case of reproduction. apple snails deposit about 157$\sim$784 (average of 321 eggs) milky white to pale orange colored eggs above the waterline. In approximately every 22.4 seconds a new egg appears. The total time needed to deposit a egg mass varies from 58 minutes$\sim$4 hours 13 minutes. Apple snails reproduct actively from May to June and from September to October. An appetite of apple snails for rice plants was the different depending on their size and glowing stage for rice plants. Apple snails had a great appetite of rice plants as well as dropwort, tomato, cabbage, radish, aquatic plants etc. They preferred to eat young rice plants and drastically quit eating rice plants of over 40 cm in height. Thus considering the food preference of apple snail for various plants including rice, they were thought to be a potentially strong predator in fields, especially, at regions with warmer winter.

• Korean journal of applied entomology
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• v.56 no.2
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• pp.97-105
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• 2017

An investigation was conducted to determine the characteristics of seasonal occurrences and effective insecticides for minimizing the occurrence of Pseudaulacaspis cockerelli in sweet persimmon orchards. Most of the nymphs or female scales that mated in mid-September overwintered on twigs, matured to lay eggs in the next spring in accordance with temperature increase, and survived till mid to late May to lay all of their eggs. Males mostly died after mating by the end of September, while the males on the fallen leaves died during the hibernating period. Egg laying in P. cockerelli showed differences in accordance with the weather conditions in each year. They laid eggs from mid-April to mid- or late May, with a peak in early or mid-May. A female was estimated to lay 160 eggs; eggs hatched a week later from the peak period of egg laying. In summer, egg laying started in early or mid-July and ended in mid- or late August, with a peak in late July or early August; a female laid approximately 130 eggs in summer. The estimated egg period was 4 days. The first generation nymph that hatched from the eggs laid by the overwintered female on twigs showed 10% occurrence on twigs and 90% on leaves. The first generation nymphs on twigs mostly developed into female scales. The occurrence of the second generation nymphs reached a peak on July 27, 2009; they lived on the twigs as their overwintering site from mid- or late August. The female and male scales on leaves developed at the similar rate as the first generation nymphs up to August. The occurrence of male scales indicated that the peak occurrence of nymphs was on August 12, 2009, male scales on August 27, and adults approximately on September 14, which showed steady relationship in the sequence of development from nymphs to adult males. Among the nymphs that occurred on the leaves on August 12, 75% of them emerged into male adults, mated, and died. Buprofezine+dinotefurn (20+15) WP treatment on June 9 and 16 resulted in 90.6% control of P. cockerelli, when mortality was checked 7 weeks after treatment.

• Korean journal of applied entomology
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• v.55 no.4
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• pp.453-457
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• 2016

This study investigates the hatching periods and hatchability of the eggs of Pochazia shantungensis at different collection times from 2011 to 2014, and the effect of temperature on the growth of P. shantungensis nymphs in an area of its outbreak. The hatchability of P. shantungensis eggs varies with their collection time; their hatchability in late November was higher than that in March of the next year, but no difference was observed in their hatching periods. The hatching periods of the eggs were 51.2, 31.3, 24.8, 19.4, 17.1, and 19.4 days at 15, 18, 21, 24, 27, and $30^{\circ}C$, respectively. The hatchability was above 70% at temperatures ranging from 18 to $27^{\circ}C$. The hatching time of the overwintered eggs in the Gurye region in Korea was reduced by 9 days from 2011 to 2014. The hatching rate was relatively higher when the average temperature in the winter season was relatively warmer. The dvelopmental periods of the first to fifth nymphs were 82.8, 58.0, 45.8, and 39.6 days at 18, 21, 24, and $27^{\circ}C$, respectively, at the relative humidity of 40~70%, and a photoperiod off 14 h light:10 h dark. The higher the temperature, the shorter the developmental period. At $30^{\circ}C$, all life stages after the fourth nymph died. Thus, the optimum growth temperature was estimated to be $27^{\circ}C$. For all life stages from the egg to the fourth nymph, the relationship between the temperature and developmental rate was expressed by the linear equation Y = 0.0015 X - 0.014. The lower developmental threshold was $9.3^{\circ}C$ and the effective cumulative temperature was 693.3 degree-days. The lower developmental threshold of approximately $3.8^{\circ}C$ was the lowest at the fourth nymph stage.