粤北晚稻褐飞虱发生动态

【目的】粤北地区是褐飞虱Nilaparvata lugens(St?l)(BPJ)后期回迁重点区域。阐释后期褐飞虱回迁对粤北稻区的影响,可为其预测预报提供依据。【方法】利用轨迹分析平台HYSPLIT对2006—2012年粤北地区秋季回迁的褐飞虱主要峰次进行轨迹模拟,用气象制图工具Gr ADS分析2011年粤北褐飞虱回迁的降落机制,解析粤北地区后期回迁褐飞虱虫源地及其降落机制。【结论】(1)粤西北地区主要虫源地分布于湖南南部、福建南部和江西,粤东北地区虫源地主要分布于江西南部、福建南部以及广东东南沿海稻区。其中,地形因素是造成两地虫源差异的主要原因。(2)通过粤北地区2011年秋季几个迁入高峰日各气象要素分析结果显示,低空急流能为主降区输入褐飞虱虫源;低层切变线和强降雨过程是造成粤西北褐飞虱大规模降落的主要因素。(3)2011年粤北晚稻褐飞虱出现两个回迁高峰(8月下旬至9月上旬、9月下旬至10月上旬),随着晚稻进入分蘖抽穗期,良好的食料条件加之两次较大的回迁峰加重了褐飞虱对晚稻的危害。(4)8—9月份虫源地适宜的温度以及降水条件造成褐飞虱增殖暴发重要气候因素。     

粤北晚稻褐飞虱发生动态

【目的】粤北地区是褐飞虱Nilaparvata lugens(St?l)(BPJ)后期回迁重点区域。阐释后期褐飞虱回迁对粤北稻区的影响,可为其预测预报提供依据。【方法】利用轨迹分析平台HYSPLIT对2006—2012年粤北地区秋季回迁的褐飞虱主要峰次进行轨迹模拟,用气象制图工具Gr ADS分析2011年粤北褐飞虱回迁的降落机制,解析粤北地区后期回迁褐飞虱虫源地及其降落机制。【结论】(1)粤西北地区主要虫源地分布于湖南南部、福建南部和江西,粤东北地区虫源地主要分布于江西南部、福建南部以及广东东南沿海稻区。其中,地形因素是造成两地虫源差异的主要原因。(2)通过粤北地区2011年秋季几个迁入高峰日各气象要素分析结果显示,低空急流能为主降区输入褐飞虱虫源;低层切变线和强降雨过程是造成粤西北褐飞虱大规模降落的主要因素。(3)2011年粤北晚稻褐飞虱出现两个回迁高峰(8月下旬至9月上旬、9月下旬至10月上旬),随着晚稻进入分蘖抽穗期,良好的食料条件加之两次较大的回迁峰加重了褐飞虱对晚稻的危害。(4)8—9月份虫源地适宜的温度以及降水条件造成褐飞虱增殖暴发重要气候因素。     

云南省褐飞虱早期迁入虫源及其发生大气背景分析

为了探明我国西南稻区褐飞虱早期迁入种群的虫源地,为后期预测和防治提供依据,通过对2007—2016年云南植保站4—5月份褐飞虱虫情进行分析,选取出云南省勐海、芒市、江城、师宗、麻栗坡、广南6个代表性站点,利用WRF-FlexPart耦合模式对2013年、2015年和2016年这些站点的早期迁入峰进行了数值模拟,得到近年来云南省褐飞虱早期迁入虫源的虫源地。选取了2013年褐飞虱早期迁入量较大的迁入峰进行了大气背景分析,结合峰期影响褐飞虱迁飞的大气动力场、温度场和相对湿度场,探讨了影响云南省褐飞虱早期迁入的大气背景。研究结果表明:(1)近年来云南省褐飞虱迁入的虫源主要来自缅甸,部分来自老挝和泰国,少数来自越南,还有极少量来自孟加拉国。(2)这一时期,当释放高度分别为1500、2000 m时,褐飞虱的迁飞高度分别集中在2216 m和2489 m,平均迁飞高度分别是2167、2454 m,从不同释放高度回推的褐飞虱迁飞高度的起伏趋势具有较好的一致性,表明模式能较好地反映系统性垂直气流和下垫面起伏对其上层三维流场和种群迁飞的影响。(3)选取2013年5月22—26日发生在云南勐海、麻栗坡和广南的一次典型褐飞虱迁入过程,分析了大气背景场对褐飞虱迁飞的影响,结果显示:受印缅低压控制或影响,高空从境外虫源区至云南降虫区有西南水平气流作为种群输送动力;温场在降虫区东北侧有"低温屏障墙"存在,阻止了种群的继续北迁;垂直速度场上虫源区有上升气流促使种群起飞迁出,降虫区有下沉气流促使种群降落;弱降水形成的拖曳下沉气流对降虫也十分有利;相对湿度场对此次迁飞过程不形成任何胁迫。     

桂东北稻区第七代褐飞虱迁飞规律及虫源分析

褐飞虱是我国水稻上的一种重要迁飞性害虫,在桂东北稻区不能越冬。近年来,作为次害代的第7代褐飞虱在桂东北稻区频繁暴发,桂东北稻区作为褐飞虱南北往返迁飞的重要通道,研究阐明该稻区第7代褐飞虱的迁飞规律及虫源分布,对第7代褐飞虱的早期预警和有效防控意义重大。利用灯光诱捕的方法研究了2007—2010年桂东北稻区褐飞虱的迁飞动态,并运用大气质点轨迹分析平台HYSPLIT(Hybrid Single-Particle Lagrangian Integrated Trajectory)和气象图形处理软件GrADS(Grid Analysis and Display System)对褐飞虱迁入、迁出峰次进行轨迹分析和气象背景分析。结果表明:(1)桂东北稻区第7代褐飞虱每年都会出现2—3次迁飞高峰,虫量高峰期主要集中在9月底至10月上旬。(2)迁入虫源主要来自江西中西部和湖南中东部稻区,从本地起飞的部分褐飞虱飞行24 h或36 h后能到达广西南部沿海、越南北部和海南等越冬区。(3)925 hPa的温度高则褐飞虱虫量高;盛行东北气流较多的年份,褐飞虱发生严重;微弱的下沉气流和无雨天气有利于褐飞虱的迁飞。     

2007年广西早稻田褐飞虱发生动态及虫源分析

褐飞虱Nilaparvata lugens(Stal)是我国水稻上的重要害虫,近年来在全国连续大暴发,给我国水稻生产造成严重的损失。广西是境外虫源迁入我国的第一站,分析其早稻田褐飞虱的种群动态和迁飞规律,对全国褐飞虱的预测预报和防治工作意义重大。采用田间系统调查与雌虫卵巢系统解剖的方法研究了2007年南宁地区早稻田的褐飞虱发生动态和世代种群特征,分析全区灯诱数据确定迁入高峰期,并运用美国NOAA网站的HYSPLIT平台对2007年广西褐飞虱早期的6段迁入高峰期进行了数值模拟和虫源地分析。结果表明:(1)2007年广西南宁地区褐飞虱在晚熟品种田的发生虫量明显高于早熟品种田,发生、危害期明显延长,为我国北方其他稻区的褐飞虱的迁入积累了充足的虫源基数。(2)确定了南宁地区的早稻田褐飞虱各发生世代的虫源性质。第2代属于大部迁入型;第3代前期属于本地繁殖,部分迁入型,后期属部分迁出型;第4代属于大部分迁出型。(3)4月下旬-5月上旬,虫源地主要分布在越南、老挝中部的地区(18°-20°N);5月中下旬,虫源地主要分布在越南、老挝较北的地区(20°-22°N),部分来自我国海南省和雷州半岛;而6月上旬桂北地区大规模迁入的虫源地主要分布在越南东北部、广西西南部;低空急流为广西褐飞虱大规模迁入提供了运载气流,而当时的降雨是迫使褐飞虱集中降落的主要原因。     

大气低温胁迫对中国褐飞虱年内初始迁入的影响

为了揭示大气低温胁迫对中国褐飞虱年内初始迁入的影响,更好地预警来自境外的褐飞虱早期迁入,通过统计2000-2017年中国华南、西南两个稻区褐飞虱年内的始见期和首次迁入峰日,逆推其迁飞轨迹和虫源区,分析大气温度场对迁飞过程产生的作用,比较了褐飞虱在我国不同稻区、不同年内初始迁入期受大气低温胁迫产生的作用差异。结果表明：（1）近年来褐飞虱初始迁入中国的时间提前,初始迁入华南稻区的时间比西南稻区早,华南稻区始见期提早可能与褐飞虱种群越冬北界北移有关。（2）西南稻区褐飞虱年内初始迁入的境外虫源主要来自缅甸,华南稻区年内初始迁入的境外虫源主要来自越南和老挝的中北部。（3）对盛行迁飞层的温场分布研究表明,在褐飞虱年内初始迁入过程中低温屏障发生的概率约为54.4%,迁入当晚降虫地的平均低温强度为13.45℃,平均降温幅度为1.88℃。其中低温胁迫在华南稻区表现更为显著（发生概率为58.3%,平均强度为13.18℃）,在始见期表现得更明显（发生概率为70.6%,平均强度为12.53℃）。     

基于WRF-Flexpart的一次褐飞虱回迁过程模拟研究

褐飞虱是影响亚洲地区水稻生产的迁飞性害虫,其远距离迁飞与种群分布会受到大气环流和局地天气条件的影响。采用WRF-Flexpart耦合模式、GIS空间分析和Vincenty方位角/距离估计等方法,选取2009年9月30日—10月7日发生在中国15个植保站的褐飞虱迁入过程,并根据模式输出、GIS分析和轨迹计算结果探讨了多种大气物理胁迫共存下大气动力场、降水、温度场和湿度场对褐飞虱秋季回迁过程及其降落虫量分布的影响。研究结果表明:(1)此次重大迁飞过程中,大气动力场、降水、温度场和湿度场在不同地区、不同时间段对褐飞虱种群的迁入和降落起了不同的作用,因而造成了迁入虫量分布的时空差异。(2)从各虫源地迁出的褐飞虱种群是向着温暖而湿润的地方迁飞的,迁飞方向主要受所经区域盛行风向的影响,迁飞距离由途径区的风速所决定。(3)当迁飞种群途径局地降水较多的区域时,初期迁入量并不多,经过短暂的一段时间后降虫量会突然增加。(4)在一定的温度范围内,大气湿度条件会影响褐飞虱的迁入虫量:褐飞虱迁入虫量在近地面温度高于26℃、相对湿度(925 hPa)大于70%且下沉气流较强的地区分布最多,而在近地面温度低于24℃、相对湿度(925 hPa)小于50%、无明显下沉气流的地区未发现有褐飞虱的迁入。     

长江中游稻区夏季飞机航捕迁入褐飞虱的轨迹分析

根据1977～1979年3年的7月份飞机航捕褐飞虱Nilaparvata lugens的资料, 应用轨迹分析模型,得出了长江中游稻区夏季迁入褐飞虱的中尺度虫源地及迁入路径。1）湘东北-鄂东南稻区虫源来自桂中至湘中稻区（24°～ 28°N,109°～114°E）,褐飞虱的迁入路径有两条：①柳州→桂林→衡阳→该区;②柳州→桂林→邵阳→该区。2）赣北-鄂东稻区虫源来自桂中至赣西稻区（24°～29°N,110°～115°E）,褐飞虱的迁入路径有一条：蒙山→倏县→宜春→该区。3）湘中、东部稻区虫源来自桂南至湘南稻区 （23°～27°N,109°～113°E）,褐飞虱的迁入路径有一条：南宁→柳州→桂林→该区。     

季风进退和转换对中国褐飞虱迁飞的影响

利用近30年NCEP/NCAR 逐日气象再分析资料及中国褐飞虱逐候灯诱数据,分析季风指数与褐飞虱迁入量的时空关系,以探明季风进退和转换对我国褐飞虱迁入的影响。研究表明:(1)常年3月中、下旬是我国偏北季风转换为西南季风的时期,西南季风开始后的4月上旬是褐飞虱第1次大规模北迁的时期,第1次大规模北迁的主降区为华南稻区和西南稻区,随后迁向其北的其他稻区。(2)6月中旬-8月中旬是偏南季风指数达最大值的时期,也是各稻区褐飞虱北迁峰次最多、迁入量最集中的时期。(3)8月下旬至9月中旬为偏南季风向偏北季风的转换时期,也是褐飞虱北迁的终见期、南迁的始见期,第1次大规模南迁发生在这一时期内,主降区为江淮稻区和江岭稻区。(4)9月下旬至10月中旬是偏北季风的快速增强期、偏南季风的快速衰退期,也是褐飞虱南迁的高峰期。(5)10月下旬开始偏南季风撤出我国大陆,而偏北季风控制我国大陆,由北到南各稻区依次开始出现褐飞虱迁入的终见期。(6)褐飞虱异常发生年份中西南季风北上的早迟决定了褐飞虱在我国迁入始见期的早晚,而偏北季风南下的早迟则决定了我国褐飞虱迁入终见期的早晚。(7)迁入始见期滞后于西南季风的变化,迁入终见期滞后于偏北季风的变化,它们滞后的时间都为1-3候(即5-15d)。     

台风莫兰蒂对褐飞虱迁飞的影响

通过对2010年10号台风莫兰蒂(Meranti)进行流场分析和过程分析,阐明了此次台风对浙江稻区9月上中旬褐飞虱Nilaparvata Lugens(Stl)的迁飞造成的影响。结果表明:(1)台风过境前,其外围前方的强东南气流及高空下沉气流为褐飞虱提供了运载工具和降落条件,虫源基本来自浙江东南部和迁入区附近区域;(2)台风过境时,由于天气恶劣,部分站点上灯虫量很小,但金华和遂昌处于台风眼范围内,天气较好,风速较小,为之前随大风和降雨迁入的大量虫群提供上灯的机会,造成上灯高峰,虫源地主要来自浙江省南部;(3)台风过境后,受台风后部西南风和降雨影响,福建中北部和南部有褐飞虱随降雨迁入浙江稻区,但虫量较小。(4)根据浙江为东部临海的地理位置和台风的气旋式辐合流场的特点,从本研究结果看,莫兰蒂台风的影响仅为中小尺度范围。     

Collagen-like triple helix formation of synthetic (Pro-Pro-Gly)10 analogues: (4(S)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10, (4(R)-hydroxyprolyl-4(R)-hydroxyprolyl-Gly)10 and (4(S)-fluoroprolyl-4(R)-fluoroprolyl-Gly)10.

For the rational design of a stable collagen triple helix according to the conventional rule that the pyrrolidine puckerings of Pro, 4-hydroxyproline (Hyp) and 4-fluoroproline (fPro) should be down at the X-position and up at the Y-position in the X-Y-Gly repeated sequence for enhancing the triple helix propensities of collagen model peptides, a series of peptides were prepared in which X- and Y-positions were altogether occupied by Hyp(R), Hyp(S), fPro(R) or fPro(S). Contrary to our presumption that inducing the X-Y residues to adopt a down-up conformation would result in an increase in the thermal stability of peptides, the triple helices of (Hyp(S)-Hyp(R)-Gly)(10) and (fPro(S)-fPro(R)-Gly)(10) were less stable than those of (Pro-Hyp(R)-Gly)(10) and (Pro-fPro(R)-Gly)(10), respectively. As reported by B?chinger's and Zagari's groups, (Hyp(R)-Hyp(R)-Gly)(10) which could have an up-up conformation unfavorable for the triple helix, formed a triple helix that has a high thermal stability close to that of (Pro-Hyp(R)-Gly)(10). These results clearly show that the empirical rule based on the conformational preference of pyrrolidine ring at each of X and Y residues should not be regarded as still valid, at least for predicting the stability of collagen models in which both X and Y residues have electronegative groups at the 4-position.     

Synthesis and luminescence properties of a blue-emitting Sr(3.5) Y(6.5) O(2) (PO(4) )(1.5) (SiO(4) )(4.5) :Eu(2+) phosphor

A novel blue‐emitting Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:Eu²⁺ phosphor was synthesized via a solid‐state reaction. Powder X‐ray diffraction (XRD) analysis demonstrated that the Sr_3.5Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5 host had a hexagonal crystal structure in the space group P6₃/m and unit cell parameters a = 9.418 Å, c = 6.900 Å. The as‐prepared phosphor showed a blue emission and all the main emission peaks were located at around 466 nm for different excitation wavelengths of 297, 333 and 391 nm. The temperature dependence of the photoluminescence property was investigated in the range 20–250 °C, and the emission intensity decreased to 71% of the initial value at room temperature on increasing the temperature to 150 °C. According to the classical theory of fluorescent thermal quenching, the activation energy (ΔE) for the thermal quenching luminescence of the as‐prepared Sr_3.45Y_6.5O₂(PO₄)_1.5(SiO₄)_4.5:0.05Eu²⁺ phosphor was determined to be 0.20 eV. Copyright © 2011 John Wiley & Sons, Ltd.     

Role of tfdC(I)D(I)E(I)F(I) and tfdD(II)C(II)E(II)F(II) gene modules in catabolism of 3-chlorobenzoate by Ralstonia eutropha JMP134(pJP4)

The enzymes chlorocatechol-1,2-dioxygenase, chloromuconate cycloisomerase, dienelactone hydrolase, and maleylacetate reductase allow Ralstonia eutropha JMP134(pJP4) to degrade chlorocatechols formed during growth in 2,4-dichlorophenoxyacetate or 3-chlorobenzoate (3-CB). There are two gene modules located in plasmid pJP4, tfdC(I)D(I)E(I)F(I) (module I) and tfdD(II)C(II)E(II)F(II) (module II), putatively encoding these enzymes. To assess the role of both tfd modules in the degradation of chloroaromatics, each module was cloned into the medium-copy-number plasmid vector pBBR1MCS-2 under the control of the tfdR regulatory gene. These constructs were introduced into R. eutropha JMP222 (a JMP134 derivative lacking pJP4) and Pseudomonas putida KT2442, two strains able to transform 3-CB into chlorocatechols. Specific activities in cell extracts of chlorocatechol-1,2-dioxygenase (tfdC), chloromuconate cycloisomerase (tfdD), and dienelactone hydrolase (tfdE) were 2 to 50 times higher for microorganisms containing module I compared to those containing module II. In contrast, a significantly (50-fold) higher activity of maleylacetate reductase (tfdF) was observed in cell extracts of microorganisms containing module II compared to module I. The R. eutropha JMP222 derivative containing tfdR-tfdC(I)D(I)E(I)F(I) grew four times faster in liquid cultures with 3-CB as a sole carbon and energy source than in cultures containing tfdR-tfdD(II)C(II)E(II)F(II). In the case of P. putida KT2442, only the derivative containing module I was able to grow in liquid cultures of 3-CB. These results indicate that efficient degradation of 3-CB by R. eutropha JMP134(pJP4) requires the two tfd modules such that TfdCDE is likely supplied primarily by module I, while TfdF is likely supplied by module II.     

Induction of in vitro flowering in Dendrobium Madame Thong-In (Orchidaceae) seedlings is associated with increase in endogenous N(6)-(Delta (2)-isopentenyl)-adenine (iP) and N (6)-(Delta (2)-isopentenyl)-adenosine (iPA) levels

We analysed the endogenous cytokinin levels of Dendrobium Madame Thong-In seedlings grown in vitro during vegetative and flowering-inductive periods. HPLC was used to fractionate the extracts and radioimmunoassay (RIA) was used for assay of zeatin (Z), dihydrozeatin (DZ), N(6)-(Delta(2)-isopentenyl)-adenine (iP) and their derivatives. Coconut water used in experiments was found to contain high level (>136 pmol ml(-1)) of zeatin riboside (ZR). Protocorms and seedlings cultured in medium with coconut water were found to contain 0.5-3.9 pmol g(-1) FW of the cytokinins analysed. Seedlings (1.0-1.5 cm) cultured in flowering-inductive liquid medium containing 6-benzyladenine (BA, 4.4 muM) and coconut water (CW, 15%) contained up to 200 and 133 pmol g(-1) FW of iP and iPA, respectively. These levels were significantly higher than all other cytokinins analysed in seedlings of the same stage and were about 80- to 150-folds higher than seedlings cultured in non-inductive medium. During the transitional (vegetative to reproductive) stage, the endogenous levels of iP (178 pmol g(-1) FW) and iPA (63 pmol g(-1) FW) were also significantly higher than cytokinins in the zeatine (Z) and dihydrozeatin (DZ) families in the same seedlings. Seedlings that grew on inductive medium but remained vegetative contained lower levels of iPA. The importance of the profiles of iP and its derivatives in induction of in vitro flowering of D. Madame Thong-In is discussed.     

The helix-coil transitions of poly (dA)-poly (dT) and poly (dA-dT)-poly (dA-dT)

Helix–coil transition curves are calculated for poly (dA) poly(dT) and poly (dA-dT) poly (dA-dT) using the integral equation approach of Goel and Montroll.⁵ The transitions are described by the loop entropy model with the exponent of the loop entropy factor, k, remaining an arbitrary constant. The theoretical calculations are compared with experimental transition curves of the two polymers. Results indicate that the stacking energies for these two polymers differ by about 1 kcal/mole of base pairs. Also, a fit between theory and experiment was not possible for k > 1.70.     

Biology of Bactrocera (Zeugodacus) tau (Walker) (Diptera: Tephritidae)

The biology of the fruit fly Bactrocera tau, an important horticultural pest, was studied under laboratory conditions at 25°C and 60–70% relative humidity on Cucurbita maxima. The duration of mating averaged 408.03 ± 235.93 min. After mating, the female fly had a preoviposition period of 11.7 ± 4.49 days. The oviposition rate was 9.9 ± 8.50 eggs and fecundity was 464.6 ± 67.98 eggs/female. Eggs were elliptical, smooth and shiny white, turning darker as hatching approached, and measured 1.30 ± 0.07 mm × 0.24 ± 0.04 mm. The chorion has polygonal microsculpturing and is species-specific with polygonal walls. The egg period lasts for 1.3 ± 0.41 days. The duration of the larval period is 1.2 ± 0.42, 1.7 ± 0.48 and 4.0 ± 0.94 days for first, second and third instars, respectively. Pupation occurs in the sand or soil and pupal periods are 7.0 ± 0.47 days. The life cycle from egg to adult was completed in 14.2 ± 1.69 days; the longevity of mated females and males was 130.33 ± 14.18 and 104.66 ± 31.21 days, respectively. At least two to three generations were observed from June 2008 to June 2009.     

Spectroscopic investigations of Er(3+) :CdO-Bi(2) O(3) -B(2) O(3) glasses

This article reports on the optical properties of Er³⁺ ions doped CdO–Bi₂O₃–B₂O₃ (CdBiB) glasses. The materials were characterized by optical absorption and emission spectra. By using Judd–Ofelt theory, the intensity parameters Ω_λ (λ = 2, 4, 6) and also oscillatory strengths were calculated from the absorption spectra. The results were used to compute the radiative properties of Er³⁺:CdBiB glasses. The concentration quenching and energy transfer from Yb³⁺–Er³⁺ were explained. The stimulated emission cross‐section, full width at half maximum (FWHM) and FWHM × values are also calculated for all the Er³⁺:CdBiB glasses. Copyright © 2011 John Wiley & Sons, Ltd.     

Cationic (tripyrrinato)palladium(II) complexes

The formation of cationic palladium(II)complexes [TrpyPd^II]⁺X⁻ by salt metathesis of the respective trifluoroacetates with different salts of weakly coordinating anions X⁻ was investigated. With non-hydrolizable counterions, cationic mono- and dinuclear complexes are observed depending on the nature of the anion X⁻ and the solvent. The mononuclear cations, which are only formed with X = BAr^F, most probably carry a weakly bound molecule of dichloromethane at the fourth coordination site of Pd^II. When treated with diazoalkanes, only these are sufficiently reactive to form carbene complexes. Four- and five coordinate Lewis base adducts [TrpyPd^IIL]⁺ with L = CH₃NC, tBuNH₂, PMe₃, PEt₃ and PiPr₃ and [TrpyPd^IIL₂]⁺ with L = PMe₃ were prepared from the mononuclear cations [TrpyPd^II]⁺BAr^F−. From structural studies it becomes apparent, that the formation of stable five coordinate Pd^II species is restricted to medium size ligands and depends on the delicate balance between the steric influence of L and the strain, which is induced on the TrpyPd^II unit.