溴氰菊酯和甲胺磷引起稻飞虱再猖獗问题的研究

室内测定和田间试验的结果表明,溴氰菊酯引起稻飞虱再猖獗的现象非常明显,其原因首先是稻飞虱对溴氰菊酯具有极高的自然耐药力,连续施药以后,耐药力还会进一步提高;其次是药剂会使飞虱的产卵量增多,并杀伤天敌。这种再猖獗在用药量偏低时更为明显。甲胺磷在常用剂量下,对飞虱的再猖獗不明显。     

氮肥促进Bt水稻和非Bt水稻上溴氰菊酯诱导的褐飞虱再猖獗能力

【目的】褐飞虱Nilaparvata lugnes是Bt水稻上重要的非靶标害虫之一,多种药剂会引起褐飞虱的再猖獗。本研究旨在探究氮肥使用下Bt水稻上褐飞虱对农药的生态适应性和再猖獗能力。【方法】取Bt水稻T1C-19(含cry1C*基因)和T2A-1(含cry2A*基因)稻苗分别施以0,100和250kg N/hm~2的氮肥,用不同浓度溴氰菊酯(0,1,3和6 mg/L)喷雾处理其上饲养的褐飞虱,分析氮肥处理的Bt水稻上褐飞虱对农药的生态适应性指标(若虫发育历期、若虫存活率、雌成虫体重、单雌产卵量和卵孵化率)。【结果】高浓度溴氰菊酯(6 mg/L)处理下褐飞虱的若虫存活率显著低于未处理组,而单雌产卵量则高于未处理组。方差分析表明,氮肥与溴氰菊酯相互作用可以显著影响褐飞虱的若虫存活率、雌成虫体重、单雌产卵量和卵孵化率。在0 kg N/hm~2处理下,溴氰菊酯处理对褐飞虱的产卵量无显著影响。在100和250 kg N/hm~2处理稻株上褐飞虱产卵量随着溴氰菊酯浓度的升高而增加。随着氮肥施用量的增加,褐飞虱若虫历期缩短,雌成虫体重增加,产卵量增加,褐飞虱若虫孵化率和存活率增高。相同氮肥施用量、溴氰菊酯同一浓度处理条件下,Bt水稻和常规水稻相比对褐飞虱的若虫发育历期、产卵量、卵孵化率和存活率均无显著影响。【结论】本研究结果表明,氮肥可以促进Bt水稻和非Bt水稻上溴氰菊酯诱导的褐飞虱再猖獗。     

闽北地区稻飞虱和黑尾浮尘子初步研究

稻飞虱和浮尘子是我省的主要水稻害虫,历年各地普遍发生,均有不同程度的为害,尤其近年来,为害猖獗,严重性超过螟害,而成为水稻的首要害虫,为了保证水稻的丰产,1958年我们对此虫进行了初步的调查和研究。兹将所得结果整理于后,以供参考。 一、种类 根据田间调查和预测灯下记载资料,目前发现稻飞虱种类有:白背飞虱、褐飞虱、粉白飞虱、绿飞虱、黑头麦飞虱等5种;浮尘子有:白翅浮尘子、黑尾浮尘子、电光浮尘子、两点黑尾浮尘子、两点浮尘子、大浮尘子、小绿浮尘子、苦楝浮尘子、麻色浮尘子等9种。飞虱中以白背飞虱和褐飞虱数量最多,其中又以白背飞虱较     

转Bt基因及其亲本水稻上褐飞虱对三唑磷和溴氰菊酯的反应

以转Bt基因抗虫水稻T1C-19(含cry1C基因)和T2A-1(含cry2A基因)及其亲本水稻MH63为材料,用20和40 mg·L^-1的三唑磷以及1、3和6 mg·L^-1的溴氰菊酯喷雾分别处理稻株上的3龄褐飞虱若虫,研究了两种农药对转Bt基因抗虫水稻上褐飞虱再猖獗的影响.结果表明： 三唑磷处理对褐飞虱的若虫历期无显著性影响,溴氰菊酯则能显著降低若虫历期,但随着两种药剂处理浓度的升高,若虫的存活率降低、成虫的产卵量增加.在同一浓度农药药剂处理下,3个水稻品种上的褐飞虱若虫发育历期、若虫存活率、初羽雌成虫体质量、产卵量和卵孵化率等生态学参数均没有显著差异.表明褐飞虱在两种转Bt水稻上对三唑磷和溴氰菊酯诱导再猖獗的反应能力与其亲本水稻MH63没有差异.     

转基因抗虫杂交稻对非靶标害虫稻飞虱田间种群动态的影响

以常规稻Ⅱ优明86为对照,研究了转双价基因(cry1Ac SCK)抗虫杂交稻Ⅱ优科丰6号对稻飞虱田间种群的影响。采用吸虫器法调查结果表明,Ⅱ优科丰6号在水稻的整个生育期内,对白背飞虱Sogatella fucifera、褐飞虱Nilaparvata lugens种群及飞虱若虫群体均未产生显著影响;田间卵量剥查镜检结果表明,Ⅱ优科丰6号生长前期对白背飞虱的产卵有一定的吸引和刺激作用,而后期对褐飞虱的产卵有一定的拒避和抑制作用,但从整个生育期来看对飞虱的产卵行为无显著影响。因此,从短期研究结果分析,Ⅱ优科丰6号对非靶标害虫稻飞虱田间种群表现安全,同时也未引起稻飞虱田间种群猖獗。     

介绍一种稻飞虱取食量测定方法

<正> 测定稻飞虱在稻株上的取食量是研究水稻对稻飞虱抗性的手段之一,其原理是通过测定一定时间内飞虱排泄蜜露的数量,判断其取食多寡,作为评价不同水稻品种对稻飞虱抗性的依据之一。     

利用普通野生稻褐飞虱抗性改良水稻恢复系的研究

褐飞虱是我国水稻主要害虫之一,挖掘和利用稻飞虱抗性基因,选育抗稻飞虱的水稻品种是目前防治褐飞虱最科学、安全的一种措施。本研究利用具有高抗褐飞虱显性基因的抗源材料HS204作为抗源供体,以恢复系明恢65、582、MR等作为轮回亲本,通过回交,苗期群体鉴定和成株期农艺性状选择,成功地将高抗褐飞虱基因转育到轮回亲本中,获得45份抗性纯合株系,同时其配合力、米质等其他农艺性状也得到了相应改善。     

基于移动终端的稻田飞虱调查方法

【目的】建立一种基于移动终端的稻田飞虱调查方法,以减轻测报人员劳动强度,提高稻田飞虱调查的客观性,实现稻飞虱调查结果可追溯。【方法】利用Android相机、可伸缩手持杆和装载控制相机APP的Android手机研制了稻田飞虱图像采集仪。在Android开发环境下,利用socket通信和视频编码等技术,实现Android相机的视频采集与编码模块、视频传输模块和相机命令控制模块等。利用Android NDK开发和Java web等技术,实现手机端的视频预览模块、手机控制模块、图像上传模块等。相机实时拍摄的视频将压缩成H.264格式,通过RTSP/RTP协议控制其传输至手机端。手机端通过解压缩,实现实时预览相机所拍摄的视频,并控制相机拍摄水稻茎基部飞虱图像,同时将图像传输到手机端。稻飞虱识别算法部署在云服务器上。手机端可选择稻飞虱图像上传至云服务器,云服务器运行稻飞虱自动识别算法,结果返回至手机端。【结果】基于移动终端的稻田飞虱调查方法利用手机可以实时预览相机拍摄的水稻茎基部飞虱画面,控制相机拍照。云服务器上稻飞虱自动识别算法对图像中的飞虱平均检测率为86.9%,虚警率为11.2%;对稻飞虱各虫态平均检测率为81.7%,虚警率为16.6%。【结论】基于移动终端的稻田飞虱调查方法可以便捷地采集到水稻茎基部飞虱图像,实现稻田飞虱不同虫态的识别与计数。该方法可大大减轻测报人员的劳动量,避免稻飞虱田间调查的主观性,实现稻飞虱田间调查的可追溯。     

稻飞虱灾变机理及可持续治理的基础研究

稻飞虱(褐飞虱、白背飞虱和褐飞虱)是威胁我国粮食安全最大的生物灾害。本文基于稻飞虱致害能力的高度变异性、对农药的高适应性、传播病毒病和具有远距离迁飞能力等特点,以及研究中存在的稻飞虱迁飞动态、致害性变异和种间互作关系等灾变机理机制不清楚,提出了稻飞虱迁飞时空动态、致害性变异、稻飞虱传播的病毒病、农药对稻飞虱及其天敌的生态毒理效应、稻飞虱基因组数据分析和稻田生态系统对稻飞虱种群数量调控功能6个研究发展方向以阐明稻飞虱灾变的内在机理,为稻飞虱可持续治理体系建设提供理论依据。     

常见飞虱的识别

飞虱属于同翅目飞虱科,主要为害禾本科植物,其中稻飞虱是水稻上的大害虫,分布很广,常暴发成灾。飞虱科中的有些种类还能传播病毒病,如灰飞虱就是水稻黑条矮缩病和条纹叶枯病的传播媒介。由于不同种的飞虱在外形上常易混淆,即使是同种的雌雄个体在体形颜色上的差别也较大,因此正确识别飞虱的种类在测报与防治上都很重要。 通过田间调查和灯下采集,常见的飞虱主要有以下10种:     

Differential resurgence and response elimination

Resurgence refers to the transient recovery of previously reinforced, but presently not reinforced, responding when more recently reinforced responding is extinguished. The primary purpose of our research was to determine how differential resurgence results from the procedures used to eliminate that responding. There were three conditions in each of five experiments. In Condition 1, key pecking by pigeons was maintained under a two-component multiple variable-interval (VI) 30-s VI 30-s schedule. In Condition 2, this pecking was eliminated in different ways across components. In Condition 3, extinction was in effect for all responses, and resurgence of key pecking was compared across components. These three conditions were repeated for most pigeons, and the procedures used to eliminate responding in Condition 2 varied across experiments. In Experiment 1, there was greater resurgence, and an earlier onset of it, after a differential-reinforcement-of-other-behavior (DRO) schedule than after a VI schedule was correlated with pecking an alternative key. Experiments 2 and 3 showed that the differential resurgence in Experiment 1 probably was not due to conditional stimulus control or the periodicity of food delivery, respectively. In Experiment 4, there was no systematic difference in resurgence after either a DRO schedule or a VI schedule correlated with treadle pressing. In Experiment 5, there was greater resurgence, and/or an earlier onset of it, after a VI schedule correlated with treadle pressing than after a VI schedule correlated with pecking an alternative key. Taken together, the results showed that the reinforcement of an alternative key-peck response was the most effective means of reducing subsequent key-peck resurgence. The relation of these results to an understanding of resurgence is discussed.     

农药诱导害虫再猖獗机制

害虫再猖獗是农林害虫防治中出现的普遍现象,包括生态再猖獗和生理再猖獗.前者的机制主要是药剂削弱了自然控制作用,后者主要是药剂引起害虫的毒物兴奋效应及补偿作用(刺激产卵).作者团队最新研究证明,药剂刺激产卵是由于药剂激活了脂肪体RNA转录水平,使卵黄蛋白基因表达量显著上调;两性交配昆虫药剂同样刺激雄性生殖并能通过交配传导...     

Modelling pest population resurgence due to recolonization of fields following an insecticide application

1. To investigate the effect of insect recolonization on the insecticide-induced resurgence of crop pests, a modified Lotka–Volterra predator–prey model was partitioned into two areas, 'sprayed' and 'unsprayed'.
2. The unsprayed area provided a source of insects to recolonize the sprayed area, resulting in a change in pest dynamics in both areas following an insecticide application.
3. Model sensitivity to insecticide selectivity and rates of predation, insect dispersal and pest population increase were examined.
4. Resurgence risk in the sprayed area increased with increasing pest dispersal rate, but decreased with increasing predator dispersal rate.
5. Pest resurgence could also occur in the unsprayed area, especially when prey dispersal rates were low. The extent of resurgence in the unsprayed area could in some circumstances be worse than in the sprayed area itself.
6. The more efficient and longer-lived the predators, the greater the level of pest resurgence in both areas following insecticide use.
7. More selective insecticides, killing the pest, but not the predator, reduced resurgence provided that the average life-span of the predators was reasonably long. Even highly selective insecticides could cause resurgence of the pest in the unsprayed area.
8. When the prey carrying capacity of the unsprayed area was increased relative to that of the sprayed area, resurgent effects in the unsprayed area were reduced, but could still be significant under some circumstances.     

农药诱导害虫再猖獗的研究

害虫再猖獗是化学防治的3个负效应之一。农药的使用剂量、次数、使用方式以及导致植物营养变化等因素都可能引发害虫再猖獗。文章重点论述产生害虫再猖獗的原因和研究现状,并讨论再猖獗的今后研究方向。期望在害虫综合治理中能对再猖獗问题引起足够的重视。     

Resurgence: the role of extinction

Three hens were trained to door push and three were trained to head bob using food as the reinforcer (Behaviour 1 training). A period of extinction followed. Each hen was then trained to perform the other behaviour (Behaviour 2) and this was followed by seven sessions of extinction. This whole sequence was repeated six times, with two sessions of extinction following Behaviour 1 training. Over the repeated extinction conditions there were decreases in responding early in extinction, for both Behaviours 1 and 2, compared with the first condition. Behaviour in the later extinction sessions could be studied for Behaviour 2 only, and it was found to increase relative to the first condition, over repeated extinction conditions. The occurrence of Behaviour 1 during the extinction following the training of Behaviour 2, that is the resurgence of Behaviour 1, both over the whole of and in the first session of each extinction phase, was variable and tended to increase over these six conditions. Thus it is possible to study resurgence using a within-subject design but the effect of repeated extinction conditions needs to be considered. The period of extinction immediately following Behaviour 1 training was then increased to nine sessions for two replications of the whole sequence. This was followed by two repeats of the sequence with no sessions of this extinction and then by another repeat, with nine sessions of this extinction phase. Over these five conditions the total resurgence of Behaviour 1 was generally greater when there were no sessions of extinction immediately following Behaviour 1 training, than when there were nine sessions. This result was more marked for the resurgence of Behaviour 1 in the first session of the extinction of Behaviour 2. Thus, these data support the hypothesis that the resurgence of Behaviour 1 is the result of the prevention of the extinction of Behaviour 1 by training Behaviour 2. At a similar point in extinction, the number of occurrences of Behaviour 1 in its own extinction was not significantly different from the number of occurrences of Behaviour 1 during the extinction of Behaviour 2. This fails to support the hypothesis that resurgence is induced by the extinction of Behaviour 2.     

Fundamental limits on inferring epidemic resurgence in real time using effective reproduction numbers

We find that epidemic resurgence, defined as an upswing in the effective reproduction number (R) of the contagion from subcritical to supercritical values, is fundamentally difficult to detect in real time. Inherent latencies in pathogen transmission, coupled with smaller and intrinsically noisier case incidence across periods of subcritical spread, mean that resurgence cannot be reliably detected without significant delays of the order of the generation time of the disease, even when case reporting is perfect. In contrast, epidemic suppression (where R falls from supercritical to subcritical values) may be ascertained 5–10 times faster due to the naturally larger incidence at which control actions are generally applied. We prove that these innate limits on detecting resurgence only worsen when spatial or demographic heterogeneities are incorporated. Consequently, we argue that resurgence is more effectively handled proactively, potentially at the expense of false alarms. Timely responses to recrudescent infections or emerging variants of concern are more likely to be possible when policy is informed by a greater quality and diversity of surveillance data than by further optimisation of the statistical models used to process routine outbreak data.     

Effects of training history on resurgence in humans

This experiment assessed the effects of training history on resurgence in three college students. Four-choice arbitrary-matching-to-sample trials occurred in two components of a multiple schedule. An A1 or A2 sample stimulus and four (B) comparison stimuli occurred on AB trials, and a C1 or C2 sample stimulus and four (D) comparison stimuli occurred on CD trials. By the end of training, accuracy and latency measures were comparable across separate discriminations, selecting B2 in the presence of A2 and selecting D2 in the presence of C2, despite a lengthier training correlated with the former discrimination. Next, in the presence of A2 and C2, respectively, responses to B2 and D2 were extinguished and responses to B3 and D3 were reinforced. These responses to B3 and D3 then were extinguished in a final condition. In this final condition, resurgence to B2 occurred for each participant, whereas resurgence to D2 occurred for only one participant. Thus, there was greater resurgence of the discrimination with the lengthier training history, despite the discriminations being similar in terms of accuracy and latency before extinction. This result, therefore, can be classified as a latent, or remote, behavioral history effect.     

Resurgence of malaria in Bombay (Mumbai) in the 1990s: a historical perspective

Bombay has achieved extraordinary success in controlling its malaria problem for nearly six decades by relying primarily on legislative measures and non-insecticidal methods of mosquito abatement. In 1992, however, malaria reemerged in Bombay with a vengeance. During 1992-1997, the city witnessed a manifold increase in the number of malaria cases diagnosed and treated by the public health system. The large number of malaria patients treated by private practitioners was not recorded by the municipal malaria surveillance system during this period. In 1995, at the peak of the resurgence, public health officials of the Municipal Corporation of Greater Bombay (MCGB) confirmed that 170 persons in the city had died due to malaria. The crisis was unprecedented in Bombay's modern public health history. In response to intense criticism from the media, the city's public health officials attributed the resurgence to the global phenomenon of mosquito-vector resistance to insecticides, and Plasmodium resistance to antimalarial chemoprophylaxis and treatment. Local scientists who investigated the problem offered no support to this explanation. So what might explain the resurgence? What factors led the problem to reach an epidemic level in a matter of two or three years? In addressing the above principal questions, this paper adopts a historical perspective and argues that in the resurgence of malaria in Bombay in the 1990s, there is an element of the 'presence of the past'. In many ways the present public health crisis in Bombay resembles the health scenario that characterized the city at the turn of the 19th century. It is possible to draw parallels between the early public health history of malaria control in Bombay, which was punctuated by events that followed the bubonic plague epidemic of 1896, and the present-day malaria epidemic punctuated by the threat of a plague epidemic in 1994. As such, the paper covers a long period, of almost 100 years. This time-depth is used to illustrate how malaria control programs in Bombay and in other parts of India have evolved through a combination of local historical forces and political expediencies in the context of technological developments. The boom in construction activities in Bombay following the liberalization of the Indian economy in 1991, and the local politics affecting administrative practices of the MCGB, are discussed as crucial factors in the crystallization of the present-day malaria resurgence in Bombay. The paper concludes by arguing that malaria in urban India is a serious problem that cannot be neglected. In the case of Bombay, the solution to the crisis can be found, in part, by reexamining the historical and political issues that have determined the nature and magnitude of the problem over the last century.     

Regression and resurgence of the CL following PGF2alpha treatment 3 days after ovulation in mares

The present study was designed to characterize and compare the physiology and ultrasonographic morphology of the corpus luteum (CL) during regression and resurgence following a single dose of native prostaglandin F2alpha (PGF) given 3 days after ovulation, with a more conventional treatment given 10 days after ovulation. On the day of pre-treatment ovulation (Day 0), horse mares were randomly assigned to receive PGF (Lutalyse; 10 mg/mare, i.m.) on Day 3 (17 mares) or Day 10 (17 mares). Beginning on either Days 3 or 10, follicle and CL data and blood samples were collected daily until post-treatment ovulation. Functional and structural regression of the CL in response to PGF treatment were similar in both the Day 3 and 10 groups, as indicated by an abrupt decrease in circulating concentrations of progesterone, decrease in luteal gland diameter and increase in luteal tissue echogenicity. As a result, the mean +/- S.E.M. interovulatory interval was shorter (P < 0.0001) in the Day 3 group (13.2 +/- 0.9 days) than in the Day 10 group (19.2 +/- 0.7 days). Within the Day 3 group, functional resurgence of the CL was detected in 75% of the mares (12 of 16) beginning 3 days after PGF treatment, as indicated by transient major (6 mares) and minor (6 mares) increases (P < 0.05 and < 0.1, respectively) in progesterone. Correspondingly, mean length of the interovulatory interval was longer (P < 0.03) in mares with major resurgence (15.8 +/- 1.6 days) than in mares with minor (11.2 +/- 1.2 days) and no resurgences (13.5 +/- 0.3 days) in progesterone. Structural resurgence of the CL in the Day 3 group and functional and structural resurgence in the Day 10 group were not detected. In conclusion, PGF treatment 3 days after ovulation resulted in structural and functional regression of the CL and hastened the interval to the next ovulation, despite post-treatment resurgences in progesterone.