二化螟人工饲料关键因子的优化及其优化配方的饲养效果

采用5因子4水平正交试验,将作者在以前筛选出的二化螟Chilosuppressalis(Walker)人工饲料的5个关键因子进行了进一步的优化,并得出了二化螟人工饲料的优化配方,其成分如下:稻茎粉18.75g、大豆粉15.00g、麦芽粉15.00g、稻糠粉6.25g、茭白茎粉7.50g、干酪素10.00g、酵母粉18.75g、纤维素7.50g、蔗糖15.00g、葡萄糖7.50g、维生素C7.50g、复合维生素B3.00g、胆固醇0.375g、氯化胆碱0.25g、Beck氏盐2.50g、山梨酸1.35g、琼脂13.49g和自来水809.25g。通过连续3代继代饲养试验,比较了该优化配方和二化螟天然饲料水稻茎的饲养效果。结果表明,在一些关键指标上(如存活率、化蛹率和羽化率等),所优化的二化螟人工饲料配方的饲养效果明显的好于其天然饲料水稻茎的;而在许多其它的指标上(如蛹期、成虫期、产卵量、卵期和孵化率等),该优化配方对二化螟的饲养效果与水稻茎的相当;但该配方饲养的二化螟在第3代时幼虫历期明显的比水稻茎的有所延长。     

大螟人工饲养技术的初步研究

利用大豆粉、玉米粉、麦胚和鲜茭白等成分配制了大螟Sesamia inferens(Walker)的半合成人工饲料,利用该饲料配方,发展了大螟的长期、继代饲养技术,即初孵-2日龄幼虫在茭白上饲养,3日龄-化蛹在人工饲料上饲养。利用该方法连续饲养大螟3代,幼虫的发育历期、蛹重、幼虫存活率、化蛹率、羽化率、卵孵化率和单雌产卵量等生活史参数与在天然饲料茭白上饲养的大螟相比,二者没有任何显著差异。而且利用该方法饲养,成本低、省工省力,能显著减少病原菌的感染。这说明该饲养技术适于大螟种群的长期、继代饲养。     

二化螟人工饲养技术

二化螟Chilo suppressalis(Walker)是我国水稻上的重要害虫,为促进其防控技术研究,迫切需要建立二化螟标准化饲养技术。根据二化螟对关键营养成分的需求,研制了一种适合其生长发育、存活和繁殖的人工饲料配方,并发展了其长期、继代、规模化饲养的标准饲养技术。已用该饲料配方和饲养技术连续饲养二化螟69代,其适合度指标仍保持较高水平。该饲料配方和饲养技术适合二化螟的周年继代和规模化饲养,同时也为其它寡食性昆虫人工饲料的研制与开发提供借鉴和参考。     

二化螟人工饲养技术

二化螟Chilo suppressalis(Walker)是我国水稻上的重要害虫,为促进其防控技术研究,迫切需要建立二化螟标准化饲养技术。根据二化螟对关键营养成分的需求,研制了一种适合其生长发育、存活和繁殖的人工饲料配方,并发展了其长期、继代、规模化饲养的标准饲养技术。已用该饲料配方和饲养技术连续饲养二化螟69代,其适合度指标仍保持较高水平。该饲料配方和饲养技术适合二化螟的周年继代和规模化饲养,同时也为其它寡食性昆虫人工饲料的研制与开发提供借鉴和参考。     

人工饲料、转Bt水稻及其亲本稻苗饲养下二化螟种群适合度的比较研究

以人工饲料、转Bt水稻"克螟稻"(cry1Ab纯和基因型)及其对照亲本"秀水11"稻苗为供试寄主植物开展二化螟Chilo suppressalis(Walker)1～5龄幼虫的室内饲养试验,以明确不同龄期二化螟种群的生活史参数。试验结果表明:二化螟在低龄时死亡率最高。克螟稻对二化螟各个龄期表现出高抗性,其各个龄期在克螟稻上均不能化蛹,随着龄期的增加二化螟的耐受性增强。以秀水11和人工饲料饲养二化螟对其蛹期、成虫期、单雌产卵量、羽化率的影响无显著性差异,以人工饲料饲养的二化螟蛹重显著高于以秀水11饲养的二化螟的蛹重,蛹重与人工饲料饲养时间呈正相关。与秀水11幼苗相比,人工饲料饲养下有利于二化螟雌虫的分化。     

染料标记对二化螟生长发育的影响

【目的】本研究主要目的是通过染色饲料饲喂获得标记的二化螟Chilo suppressalis(Walker)成虫,且不影响其生理和行为,为二化螟成虫的扩散和运动行为提供一种标记方法。【方法】笔者所在实验室前期筛选出一个适合二化螟染料及浓度,通过连续3代饲养观察染色剂对二化螟标记效果及生长发育的影响。【结果】连续3代的幼虫期饲喂含500 mg·kg~(-1)浓度的苏丹红7B人工饲料后,幼虫、成虫及卵均可被染色,饲喂染色饲料后,其化蛹率、羽化率、成虫产卵量、寿命和卵孵化率与对照均没有显著差异。取食染色饲料的二化螟雌、雄平均蛹重比对照分别高5.3 mg和4.2 mg,雌、雄平均幼虫+蛹历期比对照延长2.8 d和2.3 d。【结论】该标记技术对二化螟没有明显的生物学影响,操作简便且经济可行,是一种较好的大规模标记二化螟的方法。     

用甜玉米粒饲养二化螟实验种群

介绍一种能够继代饲养二化螟Chilo suppressalis(Walker)实验种群的天然饲料---"甜玉米粒"及相应饲养方法。结果显示,甜玉米粒和马蹄的饲养成绩皆不同程度地高于稻苗、甘蔗和田间种群。取食甜玉米粒的幼虫存活率达92.0%,显著高于其余3种天然饲料。平均蛹重为60.7mg,单雌产卵量达197.4,除性比为0.9∶1之外,其重要生物学指标和此前报道的饲养成绩最好的马蹄没有显著差异,但成本更低,且更利于清洗消毒等加工处理,因而更适于在实际生产中大量饲养二化螟实验种群。     

甜菜夜蛾人工饲料及饲养技术研究

研究了人工继代繁殖甜菜夜蛾饲料配方及饲养方法 ,测定了各虫态发育历期、幼虫死亡率、化蛹率、羽化率、蛹畸形率及不同世代蛹重。采用改进的饲料配方饲养的深圳种群 ,第 2代幼虫死亡率、化蛹率、蛹畸形率、羽化率分别为 7 8% ,97 3 % ,2 7%和 93 8% ,第 2 ,5 ,9,1 2代平均单头蛹重分别为 1 1 9 7± 1 6 1 ,98 3± 1 1 4,94 3± 1 2 6和 82 4± 9 6mg,平均单雌产卵量分别为 1 1 3 7 2± 63 3 ,684 5± 5 3 7,45 6 9± 40 2和 3 91 7± 45 6粒。人工饲养的甜菜夜蛾 ,卵、幼虫、蛹、雌性成虫的发育历期分别为 2 5～3 5 ,1 0～ 1 2 5 ,7～ 8 5和 8～ 1 4天 ,完成一个世代需要 2 1～ 2 5天。     

利用茭白、荸荠及水稻饲养二化螟的技术研究

分别用水稻苗、茭白、水稻 +荸荠 3种方法 ,喂饲二化螟Chilosupperssalis初孵幼虫 ,比较室内 3种饲养方法对二化螟生长发育和繁殖力的影响 ,从而为二化螟的实验室饲养提供方法和依据。其中 ,在整个幼虫期用茭白饲养的二化螟幼虫发育历期和化蛹历期最短 ,分别为 ( 1 7 8± 0 5 )d和 ( 9 8± 0 8)d ,而用水稻苗饲养的二化螟幼虫发育历期和化蛹历期最长 ,分别为 ( 3 0 4± 1 2 )d和 ( 2 0 0± 1 6)d。水稻苗喂饲二化螟的雌雄蛹的比例较低 ,仅为 0 44;荸荠有利于雌性个体的分化 ,用水稻 +荸荠相结合喂饲二化螟的雌雄蛹比例为 1 1 8。用荸荠喂饲的蛹最重 (雌和雄蛹重分别为 71和 5 1mg 头 )。 3种饲养方法对二化螟的产卵率和孵化率无显著影响 ,但是 ,用水稻饲养二化螟蛹的羽化率比其它 2种饲养方法显著降低。由此可见 ,用茭白、水稻苗 +荸荠饲养方法进行二化螟饲养是切实可行的 ,它们有利于二化螟的生长发育。     

豇豆荚螟人工饲料的初步研究

本文以绿豆粉、长豇豆粉、酵母粉、多维葡萄糖、琼脂、山梨酸和甲醛为原料配制了6种人工饲料饲养豇豆荚螟Maruca testulalis Geyer,以改进其人工饲料的饲养效果。结果表明：以绿豆粉和长豇豆粉为主要原料配制的配方5和配方6饲养效果较好。尤其是配方6,豇豆荚螟的幼虫存活率和历期、蛹重和化蛹率、成虫羽化率与天然饲料饲养的豇豆荚螟相比没有差异,表明该人工饲料可用于室内人工饲养豇豆荚螟。     

亚洲玉米螟幼虫对氮、糖的吸收和利用

本文以不同含氮和含糖量的系列人工饲料为材料,研究了亚洲玉米螟Ostrinia fur nacalis(Guen6e)幼虫对氮和糖的吸收和利用。结果表明：幼虫对饲料中氮的吸收能力随虫龄增加而下降,对糖的吸收能力则随之而增强;5龄幼虫对糖的吸收能力随所食饲料中氮含量的增加而增强,而对氮的吸收则与饲料糖含量关系不大,5龄幼虫对氮和糖的消耗速率均随饲料含糖量增加而加快,但幼虫的氮利用率和虫体含氮量则随之下降;幼虫的氮消耗速率随饲料含氮量的增加而增加,而氮利用率则下降,5龄幼虫的氮利用率比3龄幼虫的氮利用率低,导致虫体含氮量的迅速下降。这些结果说明饲料中氮含量影响幼虫对糖的吸收,高龄幼虫对糖的需要量增加而对氮的需要则较稳定,饲料中糖比氮更重要。     

Effects of two artificial diets on the development and reproduction of Tirathaba rufivena (Walker) (Lepidoptera: Pyralidae)

Growth, survival, fecundity, and nutrition of Tirathaba rufivena (Walker) fed on two artificial and one natural diet were studied at 29±1°C and 75±5% relative humidity. Larvae reared on the two artificial diets showed faster growth and development, higher pupal survival and weight, and higher adult fecundity than those reared on a natural diet of young coconuts, Cocos nucifera L. The relative growth rate, efficiency of ingested food conversion, and efficiency of digested food conversion in larvae fed on artificial diets were significantly higher than those of larvae fed on young coconuts. The relative consumption rate of larvae fed on artificial diets was significantly lower than that of larvae fed on young coconuts. T. rufivena showed no significant degradation in ability to propagate after being reared on the artificial diet for five successive generations. These results indicated that two artificial diets are suitable for mass rearing of T. rufivena.     

Artificial diet for the Japanese nine‐spotted moth Amata fortunei fortunei (Arctiidae: Syntominae)

The Japanese nine‐spotted moth Amata fortunei has not been successfully reared using artificial diets. We investigated three diets for rearing A. fortunei from egg to adult: (i) leaves of common dandelion Taraxacum officinale (DL); (ii) an artificial diet used to rear the silkworm Bombyx mori (Insecta LFS^®; AD); and (iii) a mixture of AD and an artificial mouse diet (MF). The survival rate from the first instar to adult emergence on AD + MF (80.77%) was significantly higher than that on AD or DL (30.77 and 20.0%, respectively). No significant differences in developmental periods at each stage were found among the diets. Moreover, body size indices of larvae reared on AD + MF were the same as or greater than those of larvae reared on the other diets and of wild individuals. Larval nutritional indices showed that food requirements changed after the third instar; this agrees with our observations of cannibalism and survival rate. Our results suggest that AD + MF is a suitable artificial diet for A. fortunei.     

Mass rearing of the pink corn borer, Sesamia cretica Led. (Lepidoptera: Noctuidae) larvae, on semi artificial diets

The effect of two different semi-artificial diets (S.A.D1 and S.A.D2) as well as a natural corn diet on the biology and bionomics of the pink stem borer, Sesamia cretica was studied under laboratory conditions. The insect was successfully mass reared for ten successive generations at the conditions of 27 +/- 2 C degrees and 60-80% R.H. In addition, a photoperiod of 0:24 (L:D) for larvae and 12:12 (L:D) in concern to the other stages, respectively. ALong the ten successive generations, there were no significant differences between the larval periods for both the artificial diets. The S.A.D2 induced the shortest (24.0 days) larval period compared with the natural diet (27.5 days) and S.A.D1 (31.5 days). Rearing larvae on the natural diets revealed a pupal period of 11.0 days, while it was 10.0 days and 8.5 days for the artificial diets (S.A.D1) and in (S.A.D2), in respect. Moth longevity (pre-oviposition, oviposition and post-oviposition periods), to a certain extent, was affected by the larval diets. The maximal moth longevity (13.0 days) was observed for larva reared on corn plants (4, 8 and 1 days). On the other hand, the shortest period (10.5 days) of moth longevity was noticed in SAD2 (1, 9 and 0.5 days). S.A.D1 showed 11.0 days moth longevity (3,7 and 1 days). The longest oviposition period (9.0 days) was recorded in the artificial diet S.A.D2, while it was only 7.0 days in the artificial diet S.A.D1 compared with 8.0 days in case of the natural diet. The number of deposited eggs increased with the progress of the 10 successive generations (G1:G10) from 150 to 265 and from 384 eggs to 564 eggs / female for the S.A.D1 and S.A.D2, in sequence. The highest mean number of deposited eggs per female (564) was for the derived females from larvae fed on the artificial diet in G10 of S.A.D2. The rate of the deposited eggs in S.A.D2 was gradually increased (from 9.70 to 61.14% increase) more than those reared on the natural diet throughout the ten generations. The highest significant percent hatchability (92.69%) has been resulted from the artificial diet SAD2. But, it has been decreased to 85.59% in the artificial diet S.A.D1 in comparison to 65.71% in the natural diet. In addition, the significant shortest total generation period was 44.0 days resulted from the artificial diet S.A.D2, while it was 53.5 and 54.0 days for corn plants and the artificial diet S.A.D1, consequently. In short, results indicated that the S.A.D2 could be considered as a suitable artificial diet for a feasible mass rearing of the pink corn borer, Sesamia cretica led. The S.A.D2 showed the shortest larval, pupal and life span for the generation periods. Moreover, it induced the longest oviposition period and the highest mean number of deposited eggs per female and the highest significant percent of eggs hatchability/fertility. The utilization of this artificial diet (S.A.D2) would supply the researchers with high-quality insects in adequate numbers, at specified times and specific stages of development for the bioassay, toxicological and biological studies.     

Growth and induction in food consumption of Helicoverpa armigera Hbn. (Lep., Noctuidae) larvae on chickpea, soybean, and maize diets

Laboratory studies were conducted to determine the effect of different artificial diets made of powdered seed materials of chickpea ( Cicer arietinum ), soybean ( Glycine max ), and maize ( Zea mays ) on the growth, consumption, and feeding preferences of Helicoverpa armigera larvae. Food consumption and growth of ultimate instar gram pod borer larvae were minimal on maize diet. The nutritive value of the soybean diet was higher, but the consumption rate of larvae was highest on chickpea diet compared with the other test diets. The growth of larvae was statistically equal on chickpea and soybean diets, in spite of differences in the consumption rate of these diets and their nutritive value. There appears to be a direct correlation between the quantity of the diets consumed and their nutritive value for growth of the larvae on chickpea and soybean diets. The lower nutritive value of chickpea diet is correlated with its higher intake by the larvae. Similarly, the lower consumption rate of larvae on soybean diet is correlated with its higher nutritive value. The diet on which the larvae were fed during earlier instars did not induce any feeding preference for that particular diet in the ultimate larval instar. The larvae consumed similar quantities of each of the three diets in their ultimate instar, irrespective of having fed on any of these diets during any preceding instars. However, induction in the quantitative consumption of food by the larvae was evident. The higher or lower consumption rate of diet by the larvae in the ultimate instar was influenced by their food during earlier instars. Hence the food consumption rate of larvae in the last instar appears to be set while feeding on a diet in the preceding instars.     

Utilization of fatty acids by Pieris brassicae reared on artificial and natural diets

The fatty acid composition of Pieris brassicae was measured from larvae reared on four different diets. Pieris can alter the composition of fatty acids in the diet through selective incorporation and synthesis. Oleate is preferentially accumulated on artificial diets (15·9 per cent in diet, 43·8 per cent in neutral lipid (NL) of fifth instar larvae), but not equally on natural diets (18·1 per cent in Brassica napus, 25·6 per cent in the NL of fifth instar larvae). Incorporation of linolenate appears to depend on the concentration of both linolenate and linoleate in the diet. With dietary levels of 35·7% linolenate and 32·2% linoleate, fifth instar larvae contain 12·2 and 16·0 per cent, respectively, of these acids. With 45·8% linolenate and 12·5% linoleate in the diet, fifth instar larvae contain 44·1 and 11·6 per cent of these acids, respectively, in the NL. Palmitoleate is actively synthetized on the artificial diets; with trace amounts of dietary palmitoleate, fifth instar larvae have 9·3 per cent of this acid in the NL. Pieris regulates the uptake of linoleate from the diet at the intestinal wall as was shown by linoleic acid-1-¹⁴C, and is unable to convert dietary linoleate to any of the 18-carbon analogues. The female apparently accumulates linolenate into egg phospholipids on the artificial diet, but in general the fatty acid composition of the eggs resembles that of the fat body.     

Diet-switching by gypsy moth: effects of diet nitrogen history vs. switching on growth, consumption, and food utilization

Gypsy moth (Lymantria dispar (L.) (Lepidoptera: Lymantriidae)) larvae were reared from hatch on 1.25% N or 3.5% N artificial diet (previous diet) and switched reciprocally to the other diet (current diet) after molting into the second, third, fourth, or fifth instar. The nitrogen concentration of food consumed during previous instars had a strong residual effect on the growth rate in subsequent instars when a diet switch was made during instars two through four, but did not affect growth rate of fifth-instar larvae despite effects on food consumption and utilization. In early instars, larvae reared on 1.25% N artificial diet and then switched to 3.75% N diet had lower mass-adjusted growth rates than larvae continuously reared on 3.75% N diet. Conversely, larvae reared on 3.75% N diet and switched to 1.25% N had higher mass-adjusted growth rates than larvae reared continuously on 1.25% N diet. Relative to larvae previously reared on 1.25% N diet, fifth-instar male larvae previously reared on 3.75% N diet had slightly lower consumption rates, higher net growth efficiency (ECD), and higher gross growth efficiency (ECI). Larvae previously reared on 3.75% N diet tended to have lower food assimilation efficiency (AD) and lower nitrogen assimilation efficiency (AD(N)). Although both previous and current diet nitrogen concentration strongly affected larval growth and food utilization, the interaction term between these was not significant for any response variables except ECD and ECI. Because the interaction term reflects the effect of switching per se, the results indicate that there was a metabolic cost associated with switching, but no inherent net cost or benefit of diet-switching to growth.