日本応用動物昆虫学会誌
Online ISSN : 1347-6068
Print ISSN : 0021-4914
ISSN-L : 0021-4914
1 巻, 2 号
選択された号の論文の28件中1~28を表示しています
  • 原稿種別: 表紙
    1957 年 1 巻 2 号 p. Cover5-
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
  • 原稿種別: 表紙
    1957 年 1 巻 2 号 p. Cover6-
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
  • 石井 象二郎, 平野 千里
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 75-79
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    ニカメイガ幼虫の生育に必要なビタミン、アミノ酸および炭水化物についてはすでに報告してきたが、その量的要求については現在までほとんど明らかにされていない。しかし野外で稲茎を食害している幼虫の栄養を解析するためには、量的要求の決定が必要な課題であると考えられる。筆者らは炭水化物と蛋白質の含量をいろいろに変えた合成飼料で幼虫を無菌的に飼育し、一、二興味ある結果を得たので報告する。実験に用いた基礎飼料は第1表に示した通りである。これに第2表の処方に従ってブドウ糖(炭水化物源)とカゼイン(蛋白質源)を加えて飼料とした。飼育実験の結果を第3表および第1図に示した。炭水化物、蛋白質のいずれか一方でも全く欠けている飼料では、幼虫は生育できない。炭水化物、蛋白質の両方が加えられている飼料では、蛋白質が炭水化物と等量又はそれ以上存在すると幼虫の生育は良好であるが、蛋白質が炭水化物より少なくなると生育は急激に低下する。本実験で使用した飼料では、その炭水化物および蛋白質の最適含量は、それぞれ15〜40%、40〜60%の範囲にあると考えられる。各飼料(A、Iを除く)で生育した幼虫体について水分、全窒素および粗脂肪の含量を測定した結果、各成分は飼料の炭水化物ならびに蛋白質の含有量の変化に伴って著しく変化することがわかった。水分および全窒素含量は飼料中の蛋白質の増加と平行して増加し、粗脂肪含量は飼料中の炭水化物量に伴って増減する(第2図)。また幼虫体の粗脂肪含量と粗蛋白質含量、(全窒素×6.25)の和は第4表に示したように、全飼料を通じて大体一定した値、すなわち幼虫の乾燥体重の約80%を保った。このことから飼料中の炭水化物、蛋白質の量的変化に伴う幼虫体内の固形物成分の変動は、大部分脂肪と窒素化合物の量的変化によるものであり、他の成分は常にほぼ一定した含量を維持しているものと考えられる。
  • 野村 健一, 鈴木 晃
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 80-87
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    In 1954〜1956 the authors practised ecological surveys of the Long-tailed blue, Lampides boeticus L., in the B0so Peninsula of Chiba Prefecture, as the supplemental one to the study published in the previous paper (1954). In this paper they chiefly investigated the annual life cycle of the species and the migration of its adults. The results obtained are summarized as follows : 1. In the frostless region of the peninsula, hibernation of the species was recognized chiefly at stages of larvae and adults in the early seeded fields of broad beans, as well as in the fields of early harvest culture used by vernalized seeds. 2. As one of the most important factors controling the annual prevalence of occurrence of the species, the seasonal arrangement of its host plants (Fig. 2) is pointed out. The typical occurrence curve of adults in every district, classified by three kinds of broad bean culture, is considered as shown in Fig. 4 (A : early harvest culture used by vernalized seeds, B : early seeded culture, C : standard culture). 3. As for Iwase's theory with reference to the migration of adults from the hibernaton region to the northern parts in spring or summer, the authors support the theory from the four reasons. 4. It has been recognized that the flowering season of broad beans and damages in autumn and winter given by larvae have a close correlation.
  • 三田 久男
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 87-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 平野 千里
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 87-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 田中 正
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 88-94
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー

    Green peach aphid (Myzus persicae SULZER) is one of the most important pests of curciferous vegetables in Japan. It is seriously injurious to Daikon, cabbage and Petsai. Such leaves aregenerally crowded with this aphid : green, yellow and pink aphids, some winged, others wingless, and of several sizes. Green and pink forms in this paper were started from two wild colonies collected in Utsunomiya and Tokyo. The aphids were reared in a large glasshouse (average temperature 13℃) or in greenhouse (average temperature 25℃) during 1951 (except summer) and in the spring of 1952. Individual rearing. The colour variation of two coloured forms reared on a piece of cabbage leaf in a small cup was very stable under the same rearing conditions. For instance, 726 of green form and 297 of pink form of the offspring of initial female all maintained their own colour. Otherwise, the green form showed that the nymphal period was shorter and the reproductive number of young per day was larger than the pink form. Mass rearing. In 1952,the author studied the leaf-by-leaf distribution and the reproductive number of young between the green and pink forms on the potted young cabbage. The degrees of the age of leaves are distinguished on external appearance alone. [table] Figures 1 and 2 show the leaf-by-leaf distribution of the green form (open blocks) and pihk form (solid blocks) on different plants. Fig. 1 showed the results of rearing in the greenhouse (average 25℃) and Fig. 2 showed the results of rearing in the glasshouse (average 13℃). The age of each leaf at the time of counting the aphid are indicated by the length of the horizontal line on the same plants. In the greenhouse, at first, the green form was extremely dence on the younger leaf of growing plants and the pink form was sparsely crowded on the older leaf. But later, a new colony of the green form is extended on the middle and mature leaves but not the pink form.Otherwise, the number of both forms are gradually increased on the potted cabbages until the aphids are crowded to the saturation point and then a few winged or nymphs are produced by wingless female. But in the glasshouse, they did not develop into a heavy infestation like the above. And between the green and the pink form the leaf-by-leaf distribution was not clear as on the above items. The third figure gives the same results in the greenhouse at the next rearing. The Figs. 4 and 5 show that light infestations of the green and the pink form develop simultaneously on same plant, which permits a direct comparison of the distribution of the two forms in relation to leaf age. The leaf-by-leaf densities of the two forms showed that the green form prefered young leaves and the pink fonn was found on the lower leaves on which they had first infested, and later they are crowded on the newly matured leaves and even on the unfurled leaves. The synthesized results of the progress of the above counts made every other day, in principle, on the cabbage are shown in Fig. 6,in terms of the average number of aphids on the same or different plants at the same time in the greenhouse. In conclusion, the green form prefers the young leaf and the pirik form prefers the old leaf in spite of the same or different plants at same time but they crowded to saturated point on their own leaves then they extend to mature or middle leaves. In the last figure, idealized curves show the relative suitability for colonization by the green (……) and pink (--) forms. The vertical line shows the suitability for aphid infestation (the higher as arrow) and the horizontal line shows the leaf age (the older as arrow). The green form seems to be more specifically adapted than the pihk form at the high temperature but the suitability of low temperature on these aphids is not clear.1. In July of 1956,the 2nd survey of the Muridae on the island of Okushiri off the west-south coast of Hokkaido was done and Rattus

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  • 太田 嘉四夫, 高津 昭三
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 95-99
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    This investigation has been carried out in order to explain the environmental factors controlling the onset of diapause in final instar of thh rice stem borer being chiefly reared on artificial diets under aseptic condition. It was demonstrated that the larva, particularly in its middle stage, is susceptible to photoperiod. If the rice stem borer belonging to the Saigoku strain is exposed during the larval feeding period to a short day length which may range from about 8 to 14hr, it enters diapause in the final instar, while a long day from 14.5 to 16hr prevents it. In the Shonai strain however, critical day length is observed at 14.5〜15hr. It is certain that this difference is due to the adaptation to seasonal fluctuation of day length within the area of distribution. Complete darkness (probably continuous illumination as well) plays neither role of induction nor prevention of diapause. The temperature of larval stage also plays some role concerning diapause. Under the complete darkness, high temperature such as 3C℃ prevents diapause, whereas low temperature such as 20℃ induces it, but the temperature effects are masked considerably in day lengths which act as antagonistic agencies. Intermediate temperature (25℃) has no influence upon diapause. So far as this investigation goes, the effects of photoperiod and temperature on egg stage are so slight that the induction or prevention of diapause may be finally decided by the environmental condition of larval stage. In experiment where the larvae were reared on the rice plant instead of synthetic media, it seemed that the diapause was not associated with phases in the growth cycle of the host plant. From the results above mentioned, it was ascertained that photoperiod alone can cause the induction of diapause in the rice stem borer larvae of the second brood in Japan.
  • 三枝 敏郎
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 99-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 井上 平, 釜野 静也
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 100-105
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    This investigation has been carried out in order to explain the environmental factors controlling the onset of diapause in final instar of thh rice stem borer being chiefly reared on artificial diets under aseptic condition. It was demonstrated that the larva, particularly in its middle stage, is susceptible to photoperiod. If the rice stem borer belonging to the Saigoku strain is exposed during the larval feeding period to a short day length which may range from about 8 to 14hr, it enters diapause in the final instar, while a long day from 14.5 to 16hr prevents it. In the Shonai strain however, critical day length is observed at 14.5〜15hr. It is certain that this difference is due to the adaptation to seasonal fluctuation of day length within the area of distribution. Complete darkness (probably continuous illumination as well) plays neither role of induction nor prevention of diapause. The temperature of larval stage also plays some role concerning diapause. Under the complete darkness, high temperature such as 30℃ prevents diapause, whereas low temperature such as 20℃ induces it, but the temperature effects are masked considerably in day lengths which act as antagonistic agencies. Intermediate temperature (25℃) has no influence upon diapause. So far as this investigation goes, the effects of photoperiod and temperature on egg stage are so slight that the induction or prevention of diapause may be finally decided by the environmental condition of larval stage. In experiment where the larvae were reared on the rice plant instead of synthetic media, it seemed that the diapause was not associated with phases in the growth cycle of the host plant. From the results above mentioned, it was ascertained that photoperiod alone can cause the induction of diapause in the rice stem borer larvae of the second brood in Japan.
  • 湯嶋 健
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 105-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 三田 久男
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 105-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 里見 綽生
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 106-112
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    To throw light upon the complex relations between the rice weevils, Calandra oryzae L. and C. sasakii TAKAHASHI, and among their geographical strains, the author compared some physiological and ecological characteristics of 10 strains of both species which were collected from different districts of the world. The strains used in the experiment are as follows : C. oryzae from Celebes (CB), Portugal (Po), Japan (JL), Siam (SH), and C. sasakii from Nepal (NE), Canada (CA), Australia (AU), Formosa (Fo), Argentine (Rz) and Japan (Js). On each species, differences in body size among strains are associated with those in some other characteristics, as tabulated in the following. The following sort of parallel variation is exhibited by C. sasakii : when the body size is small, the ratio of the adult longevity at high density to low density is large, the ratio of the rate of reproduction at high density to low density is large, and that at 33℃ to 30℃ is large. In C. olyzae these characteristics give reversal of the association with body size in C. sasakii. It is supposed that these strains represent two series of differentiation of respective species. Furthermore, the differentiation in C. sasakii from the larger sized strain to the smaller one seems to be directed towards the adaptation to the life in stored products.[table]
  • 大内 実
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 113-118
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    Observations were made on the means of hatch, the periodical variation of the number of hatching of egg masses, percentage of hatch, and the length of egg and larval stages of the rice stinkbug, Lagynotomus assimulans DISTANT from l951 to l953 with the following results. 1. According to the three years' observations the time required to hatch ranged from 2.5 to 9.5 days, with an average of 5.2 days at a mean temperature of 27.9℃ from the beginning to the middle of August. At the hatch, a black stringy triangular appendage on the abdomen supports the body and helps the larva to crawl out of the egg shell. The percentages of hatch of 60 egg masses at each five hours of day such as 1〜6 A. M., 7〜12 A.M., 1〜6P.M. and 7〜12P.M. were 56.6,21.6,10.0 and 11.6 percent respectively. In most of the egg masses, over 80 percent of eggs hatched and no parasitized egg was found. 2. The study on larvae. was successful only in August of l953 because of the difficulties in rearing. The larva passes five instars, and each period from 1st to 5th instar ranged as 2.5〜4.5 2.5〜8.5,2.5〜9.5,6.5〜13.5 and 11.5〜17.5 days successively. The average of the days required for each instar were 3.2,5.0,5.2,10.1,and 13.7 days in male, and 3.1,4.8,5.5,9.8 and 13.5 days in female. No significant difference, therefore, was observed in the period of same instar between sexes under the same condition. The mean larval period was 36.5 days in male and 35.9 days in female under the mean temperature of 22.1℃ from the middle of August to the end of September.
  • 二宮 栄一
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 119-124
    発行日: 1957/06/30
    公開日: 2017/07/19
    ジャーナル フリー
    Experiment was carried out to obtain specific data on the number of aphids destroyed by a single syrphid larva and on the rapidity of consumption of an aphid, with the following results. Table showing number of consumption of aphids. [table]Table showing average time required for consumption of an aphid.[table]
  • 小池 久義
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 124-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 田村 市太郎, 岸野 賢一, 飯島 尚道
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 125-130
    発行日: 1957/06/30
    公開日: 2017/07/19
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    Notiphila sekiyai KOIZUMI (Ephydridae) was first found in Hokuriku district of Japan in 1948 attacking the root of rice plants in te paddy field. In the present paper, the authors dealt with some morphological and ecological investigations of this insect for the purpose of its control. The results obtained are summarized as follows : 1. The eggs are laid on the leaf sheath of the rice plant as an egg-mass containing 1 to 5 eggs. An egg has dry-mud like surface, and its length is about 1.2 mm and width about 0.3 mm. Larva is yellowish milky white, its length is 7 to 8mm in its last stage and terminal segment is long and slender, about 1/5 of body length. Pupa is red brown with club like shape, and the tail part is as long as the larva. 2. Today, this insect is found to be distributed in Niigata, Toyama, Ishikawa, Shizuoka and Okayama prefectures, and is recognized to injure the rice plant in all the above districts except in Okayama prefecture. 3. It seems that the said insect has one generation a year and overwinters in the last instar of larvae . 4. The adult fly is active only in the daytime, the copulation and oviposition are observed from about 7 to 10 o'clock. The egg-mass is laid on the leaf sheath of 2 to 6cm above the water surface. Its activity is supressed in high temperature with sun shine. 5. The larva penetrates its posterior spiracle into the root tissue, and eats and cuts off the roots. Such injury continues for 25 to 30 days from the rice transplanting till it pupates. 6. The growth of rice plants injured by the larvae will be supressed and thier leaf colour fades because of the damage to the roots. Consequently, the stems do not increase and the crop yield decreases. 7. Good control results were obtained by the application of dieldrin or aldrin at the dosage of 3g per tubo (about 3.2 m^2) with 20 to 30 per cent of increase in yield as compared with the untreated ones.
  • 松沢 寛, 岡本 秀俊, 宮本 裕三
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 131-134
    発行日: 1957/06/30
    公開日: 2017/07/19
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    In order to ascertain some influences of the density of parasite progeny upon the parasite itself when the host, Pieris rapae crucivora, was attacked repeatedly by Apanteles glomeratus, the present experiment was carried out and the result was as follows : 1. The development of parasites in the host bodies seemed not to be disturbed at all in spite of the increase of the times of attacks, when the real state of emergence of the parasites from hosts and their developmental period was observed. But this was due to the fact that the calculation excepted the number of parasites whose development was disturbed and remained in the host bodies. If the calculation could be made to include the number of these unemerged parasites, we could not affirm the above explanation and we must say that the remarkable influences upon the development of parasites were brought. 2. The rate of emergence of the parasites from host bodies, the rate of cocooning, and that of emergence of adult wasps decreased remarkably with the increase of the times of attacks. Perhaps it was due to the mutual disturbance of development of the parasites in the host body when the parasite density was raised and this would be due to the high mortality of the parasites after their emergence from hosts. 3. The size of adult wasps became remarkably small and their longevity was also remarkably shortened with the increase of the times of attacks . 4. The sex ratio of the emerged wasps changed abnormally when the times of attacks were increased and the number of male wasps was larger although matured females were used for attacks in the present experiment.
  • 三田 久男
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 134-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 石倉 秀次, 伊藤 嘉昭, 宮下 和喜, 伊藤 佳信
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 135-139
    発行日: 1957/06/30
    公開日: 2017/07/19
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    In 1955 and 56,observations were conducted on the root aphids injurious to upland rice and the ants attending these aphids in the upland rice fields in Shozima city near Tokyo. The root aphids concerned were Rhopalosiphum prunifoliae, Anoecia corni and Tetraneura ulmi and the species mentioned first was more dominant than the others in June and July. Six species of ants were found in the field studied and four species, Lasius niger. Crematogaster sordidula osakensis, Pheidole fervida and Tetramorium caespitum jacoti, were observed attending the aphids. In a few cases when the soil was loose and light or there was any tunnel worked by mole cricket, the aphids seemed to go under soil without any help of ants, but there was a close positive correlation between the number of aphids and ants found in sampled soils taken at random in the fields. This correlation was observed till the middle of the season. Some ants were observed carrying the apterous female and nymphs of Rhopalosiphum prunifoliae into their hole, indicating their important role in assisting the migration of aphids from soil surface to the subterranean habitat. The frequency distribution of the numbers of both aphids and ants were not random but strongly contagious. The variance (s^2) of the average number of aphids was found to increase proportionately to their population density as shown in Fig. 1. Thus the frequency distribution of aphid numbers can be transformed into normal one if the actual numbers are changed into log_10(x+1).
  • 三田 久男
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 139-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 伊藤 嘉昭
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 140-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 宮下 和喜
    原稿種別: 本文
    1957 年 1 巻 2 号 p. 140-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 原稿種別: 付録等
    1957 年 1 巻 2 号 p. 141-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 原稿種別: 付録等
    1957 年 1 巻 2 号 p. 141-144
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 原稿種別: 付録等
    1957 年 1 巻 2 号 p. App3-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 原稿種別: 表紙
    1957 年 1 巻 2 号 p. Cover7-
    発行日: 1957/06/30
    公開日: 2017/07/19
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  • 原稿種別: 表紙
    1957 年 1 巻 2 号 p. Cover8-
    発行日: 1957/06/30
    公開日: 2017/07/19
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