白纹伊蚊种群监测与控制新技术研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
登革热或登革出血热是由蚊虫传播的一种严重危害人类健康的急性传染病,20世纪,登革热在世界各地发生过多次大流行,病例数以百万计。本论文围绕登革热的传播媒介---白纹伊蚊孕蚊种群监测和控制进行了系统的研究,并成功研制出一种针对白纹伊蚊等容器孳生型蚊虫种群监测的新型孕蚊粘捕器,弥补了目前我国白纹伊蚊监测方法中的不足,提高了白纹伊蚊的监测水平,为科学预测我国登革热疫情的流行趋势及有效控制登革热疫情提供了一定的基础。同时,为进一步提高孕蚊粘捕器的监测效果,对白纹伊蚊的产卵习性、不同浸液的产卵引诱力以及利用硫酸铜控制蚊幼虫的新方法等进行了研究,并就孕蚊粘捕器应用于白纹伊蚊等容器孳生型蚊虫的控制进行了有益的探索。本论文主要研究结果如下:
     1.孕蚊粘捕法应用于白纹伊蚊种群监测的研究
     应用新设计的孕蚊粘捕器和标准诱卵器进行的配对比较试验中,在孕蚊粘捕器所捕获的蚊虫中,白纹伊蚊占89.87%,为优势蚊种,致倦库蚊或淡色库蚊占8.87%,三带喙库蚊/伪杂麟库蚊、二带喙库蚊等占0.82%,由于主要形态鉴别特征无法识别而不能鉴定的蚊种占0.44%,蚊种构成存在显著差异;雌蚊占62.37%,雄蚊占21.58%;在解剖镜下观察,白纹伊蚊雌蚊清晰可见率为63.97%;在所粘捕的蚊虫中,96.46%的蚊虫的足跗节被粘着,蚊虫不同部位的粘附率之间存在显著的差异;86.67%的蚊虫被粘附在胶带的下部,不同粘胶部位蚊虫的粘附率存在显著差异;孕蚊粘捕法和标准诱卵器法测得的白纹伊蚊密度存在明显的正相关,两种监测结果显示的白纹伊蚊种群密度消长趋势一致。在进行的孕蚊粘捕法、诱卵法、幼虫定量计数法和人诱法比较试验中,孕蚊粘捕器的平均粘捕雌蚊数、诱卵器的平均诱集卵数和人诱法的平均成蚊数两两之间存在显著的直线相关关系。
     2.不同植物浸液对白纹伊蚊产卵行为的影响
     在室内诱卵法试验中,有绊根草浸液的诱卵杯中诱集的平均卵数为68.87,而有自来水的诱卵杯中诱集的平均卵数为23.99,两者间存在显著的差异;在室内粘捕法试验中,有绊根草浸液的诱蚊杯中粘捕平均雌蚊数为7.62,而有自来水的诱蚊杯中粘捕的平均雌蚊数为2.66,两者间存在显著的差异。在现场试验中,有绊根草浸液的孕蚊粘捕器中粘捕平均雌蚊数为5.88,而有自来水的孕蚊粘捕器中粘捕平均雌蚊数4.79,两者间差异不显著;有绊根草浸液的标准诱卵器中现场诱集的平均卵数为670.95,而有自来水的标准诱卵器中诱集的平均卵数为386.22,两者间存在显著的差异。现场试验中樟树叶、黄杨叶、狗尾草、绊根草、玉兰叶和竹叶等不同植物浸液和自来水对照没有显著的差异。
     3.白纹伊蚊产卵节律的研究
     白纹伊蚊的生殖营养周期平均为4.22天,吸血后3-4天,孕蚊卵巢发育成熟并开始产卵。室内观察白纹伊蚊产卵节律:雌蚊吸血后前2天未发现有蚊虫产卵,第3天的产卵量占总产卵量的8.22%;第4天的产卵量占总产卵量的56.41%;产卵高峰期出现在第4天,之后开始明显下降,第5天的产卵量占总产卵量的20.51%,第6天的产卵量占总产卵量的6.85%,至第10天仍有少数蚊虫产卵;白纹伊蚊的产卵活动具有明显的白昼性特点,白天的产卵量占总产卵量的91.90%,夜晚的产卵量仅占总产卵量的8.10%。现场观察其产卵节律:产卵高峰期出现在午后至傍晚的一段时间内,白天12:00-15:00,产卵量占全天总产卵量的32.51%;白天15:00-18:00,产卵量占全天总产卵量的24.95%;白天18:00-20:00,产卵量占全天总产卵量的31.86%。
     4.白纹伊蚊分散产卵行为研究
     在进行的白纹伊蚊孕蚊产卵时间分散性研究中发现:白纹伊蚊完成产卵的时间比较短,55.56%的孕蚊只需1天完成产卵,24.69%的孕蚊需要2天完成产卵,80%以上的孕蚊在1-2天内即完成产卵,也有极少数孕蚊需要6-7天才能完成产卵。设置梯度时间检查孕蚊产卵次数分布特征发现:24h检查一次,则有56.47%的孕蚊只需1次完成产卵,40.00%的孕蚊需2~3次完成产卵;3h检查一次,则34.20%的孕蚊只需1次完成产卵,42.11%的孕蚊2次完成产卵,少数孕蚊需要3-5次才能完成产卵。应用不同类型的产卵载体进行的白纹伊蚊空间分散产卵性研究发现:在产卵杯中全部为自来水的试验中,白纹伊蚊平均产卵杯数为3.66±0.19,每个产卵杯的平均产卵量百分率均低于25%;在幼虫饲养水存在的情况下,白纹伊蚊平均产卵杯数为4.18±0.19,有幼虫饲养水的产卵杯中诱集的产卵量占总产卵量的30.49±3.62%,明显多于其它有自来水的产卵杯中诱集的卵数;在有红布条存在的情况下,白纹伊蚊平均产卵杯数为3.05±0.23,在有红布条的产卵杯中诱集的产卵量占总产卵量的44.78±5.17%,明显多于其它有自来水的产卵杯所诱集的卵数;在有幼虫饲养水和红布条共同存在的情况下,白纹伊蚊的平均产卵杯数为2.03±0.12,在有幼虫饲养水和红布条的产卵杯中诱集的产卵量占总产卵量的75.95±3.14%,显著高于其它有自来水的产卵杯所诱集的卵数。
     5.金属铜或硫酸铜溶液应用于白纹伊蚊幼虫控制的研究
     在观察不同剂量金属铜浸泡不同时间的溶液对蚊幼虫或卵发育影响的试验中发现:铜离子对白纹伊蚊的幼虫发育产生明显的影响;在10g/L剂量金属铜溶液中,浸泡30天后,在放入蚊幼虫的前5天期间,幼虫发育延迟,一直维持在Ⅰ-Ⅱ龄阶段;而对照组中,第2天90%以上的幼虫发育至Ⅲ至Ⅳ龄阶段。不同剂量的金属铜溶液对白纹伊蚊幼虫均有一定的致死作用,剂量越高致死作用越明显。在40g/L剂量金属铜溶液中,浸泡至50天,放入蚊虫后的第1天,白纹伊蚊幼虫即全部死亡。铜离子对白纹伊蚊的卵发育也有一定的影响;金属铜浸泡10天后,在10 mg/L剂量金属铜溶液中,30%卵粒孵化,在20 mg/L剂量金属铜溶液中37%卵粒孵化,在40 mg/L剂量金属铜溶液中86%卵粒孵化,而对照组则有99%卵粒孵化。在进行的硫酸铜溶液对白纹伊蚊蚊幼虫或卵发育影响的试验中发现:高浓度的硫酸铜溶液对卵粒的孵化产生了显著的影响;在1 mg/L硫酸铜溶液中,加入卵粒后,第3天白纹伊蚊卵粒开始孵化,此后孵出的蚊幼虫不断增多,而在10 mg/L和100 mg/L的硫酸铜溶液中,未见白纹伊蚊卵粒孵化。高浓度的硫酸铜溶液对白纹伊蚊幼虫发育具有明显的抑制作用;1 mg/L、10 mg/L和100 mg/L的硫酸铜溶液对Ⅰ至Ⅱ龄白纹伊蚊幼虫有强烈的致死作用,蚊幼虫24h后死亡率为100%;对Ⅲ至Ⅳ龄白纹伊蚊幼虫也具有明显的致死作用,随着浓度的增加,致死作用逐渐增强;在100 mg/L的硫酸铜溶液中,至第3天,溶液中的白纹伊蚊幼虫全部死亡。在进行的硫酸铜溶液控制蚊幼虫的现场试验中发现:放置一周后,所有盛有自来水的容器内全部孳生有白纹伊蚊幼虫或蛹,而在100mg/L硫酸铜溶液的容器中,前5周均未发现蚊幼虫孳生,至第7周始,孳生蚊幼虫的阳性桶数才不断增加,硫酸铜溶液控制蚊幼虫的效果随着时间的持续而下降。
Dengue and Dengue hemorrhagic fever is a mosquito-born disease,and several major outbreaks of dengue fever have occurred in the twenty century with millions of cases.We concentrated on developing a new method to investigate and control A. albopicuts and other container-breeding mosquitoes,and suceeded in developing a new sticky ovitrap for the surveillance of A.albopictus in China.Which is very helpful to survey and control the epidemic of Dengue in China.We conducted some experiments such as studies on the oviposition pattern of A.albopictus,attractancy or repellence of the different grass or leaf infusions to the gravid A.albopictus and the new way to control A.albopictus larvae using CuSO_4 to improve the sticky ovitrap.Which could contribute to control A.albopictus and other container-breeding mosquitoes.The major results of the thesis are as followed:
     The effect of the sticky ovitrap on collecting A.albopictus(Diptera:Culicidae) in the fields were evaluated in Wuhan,China.A.albopictus accounted for 89.97%of the mosquitoes collected by sticky ovitraps,and 63.97%of them were A.albopictus with all clearly visible chracteristics.Culex quinquefasciatus or Culex pipiens pallens,Culex bitaeniorhynchus and Culex tritaeniorhynchus together made up 9.70%of mosquitoes. The percentage of unidentifiable mosquitoes was 0.44%.More A.albopictus females were collected than males,and 99.70%of tarsi of mosquitoes attached on the sticky strips were clearly visible,and the percentage of mosquitoes with the clearly visible thorax or abdomen or proboscis were 70%or so.86.67%of mosquitoes were stuck at the bottom of the sticky strips,and only few of them were stuck on the upper and middle of the sticky strips.The mean adults of A.albopictus measured by sticky ovitraps were correlated well with the mean eggs of A.albopictus detected by the standard ovitraps in 2006.The females captured by sticky ovitraps were correlated well with the eggs collected by ovitraps or the adults collected in man-biting experiments,and the linear regressions were found between eggs and females,eggs and adults,or females and adults.
     Gravid A.albopiclus laid significantly more eggs in standard red ovitraps baited with the Bermuda-grass infusion with average 68.87 eggs per ovitrap than those in the similar ovitraps containing plain tap water with average 23.99 eggs per ovitrap in the insectary, and more eggs were found in standard red ovitraps baited with the Bermuda-grass infusion with average 670.95 eggs per ovitrap than in the similar ovitraps containing plain tap water with average 386.22 eggs per ovitrap in the field.In the corresponding assays with sticky ovitraps,however,it was only in the insectary that significantly more A. albopictus female were caught in the cup using the Bermuda-grass infusion with average 7.62 females per trap than those in the cup with the tap-water with average 2.66 females per trap.While in the field there were no difference in the females captured between the Bermuda-grass infusion with average 5.58 females per trap and the tap-water control with average 4.79 females per trap.There were no difference in collecting A.albopictus female between any of six infusions made from the leaves of the camphorwood tree (Cinnamomum camphora),box(Buxus sinica var.insularis),green bristle grass(Setaria viridis),bermuda grass,lotus magnolia(Magnolia grandiflora) or a bamboo (Phyllostachys pubescens) with tap water in the field.
     The gonotrofic circle of A.albopictus wass ca.4 days,the gravid female began to lay eggs after 3-4 days bloodfed.The peak of oviposition occurred in the fourth day with 46.64%eggs being laid.Since then the gravid female decrease to lay eggs greatly with only 6.85%eggs laid in the sixth day,and a few female kept laying eggs in the tenth day. Oviposition of A.albopictus from Wuhan was almost exclusively diurnal with 91.90% eggs being laid during the full photophase in the field.A large,well defined peak of oviposition(comprising about 56.25%eggs laid) occurred in the laboratory during the one or two hours before sunset while a broad peak of oviposition occurred in the mid afternoon in the field with 32.51%eggs collected between 12:00 and 15:00,24.95%eggs between 15:00 and 18:00,and 31.86%eggs between 18:00 and 20:00.
     A.albopictus exhibited skip oviposition with laying eggs in instalment in several cups.55.56%of females laid eggs from one gonotrophic circle one time and 44.44%of them deposited eggs more than two times in a day during the 24h exposure.However,the proportion of females depositing eggs more than two times increased to 65.80%during the 3h exposure and only 34.20%of females deposited eggs one time.In response to 7 cups of water alone,individual A.albopictus laid eggs in 3.66±0.19 cups and the mean percent of eggs laid in any cup in the cage was not more than 25%eggs.In response to the larvae culture water in the cup No.3,the mean number of cups used by individual A. albopictus was 4.18±0.19 and the mean percent of eggs laid in the cup No.3 was 30.49±3.62%.In response to the red velour strip in the cup No.3,the mean number of cups used by individual A.albopictus was 3.05±0.23 and the mean percent of eggs laid in the cup No.3 was 44.78±5.17%.In response to the red velour strip and the larvae culture water in the cup No.3,the mean number of cups used by individual A.albopictus was 2.03±0.12 and the mean percent of eggs laid in the cup No.3 was 75.95±3.14%.
     The development of A.albopictus larvae and eggs could be affected by metallic copper.Exposed to the water infused with the dose of 10g/L of copper for 30 days,the larvae developed slowly and kept staying atⅠorⅡstage while most of larvae in the tap water developed toⅢorⅣstage in the second day.Metallic copper were poisonous to A.albopictus larvae.After being exposed to the water infused with the dose of 40g/L of copper for 50 days,All the larvae were dead at the first day.When the copper were infused for 10 days,A.albopictus eggs were placed in the infusion.30%eggs hatched for the dose of 10g/L of copper,37%eggs hatched for the dose of 20g/L of copper,and 86% eggs hatched for the dose of 40g/L of copper,while 99%eggs hatched in the tap water as control.Eggs kept hatching exposed to 1mg/L CuSO_4 while no eggs hatched exposed to 10mg/L CuSO_4 or 100mg/L CuSO_4.AllⅠorⅡlarvae were dead after 24h exposure of 1mg/L CuSO_4,10mg/L CuSO_4 or 100mg/L CuSO_4.CuSO_4 are poisonous toⅢorⅣlarvae,and all larvae were dead after 3 days exposure of 100mg/L CuSO_4.No larvae were found in the containers containing 100mg/L CuSO_4 during five weeks exposure while A.albopictus larvae were found in all the containers with tap water after one week in the field.Effect of 100mg/L CuSO_4 on controlling A.albopictus larvae decreased as time gone.
引文
1.蔡松武,何涌波,孙小康,卢文成,段金花,林立丰.灭蚊磁场诱捕蚊虫效果究,中华卫生杀虫药械,2005,15(3):167-168。
    2.陈燕清,张复春,王建,广州市978例登革热的临床特征分析,热带医学杂志,2003,3(2):190-192。
    3.陈文洲,周立文,林春燕,王家豪,赵志国,李雪东,纪元吉,崔五全,俞永新,白纹伊蚊在海南岛登革热流行中的病原学研究,海南医学,1982,(1):14。
    4.陈平雁,主编,黄浙明,副主编,SPSS13.0统计软件应用教程,人民卫生出版社.2005。
    5.崔可伦,广州地区白纹伊蚊的自育性,昆虫学报,1982,25(3):256-267。
    6.郭晓霞,赵彤言,董言德,蒋书楠,陆宝麟,白纹伊蚊经滞育卵传递登革Ⅱ型病毒的实验研究.中国媒介生物学及控制杂志,2003,14(1):9-11。
    7.郭晓霞,赵彤言,董言德,蒋书楠,陆宝麟,登革Ⅱ型病毒经白纹伊蚊滞育卵的传递,昆虫学报,2004,47(4):424-428。
    8.郭晓霞,赵彤言,董言德,白纹伊蚊干燥卵保存登革2型病毒的实验研究,寄生虫与医学昆虫学报,2007,14(1):20-23。
    9.郝宗宇,李晓红,马景芳,李克俊,王海峰,陈彦哲,李林红,张爱梅,孙建伟,河南预防医学杂志2006,17(1):62-63。
    10.黄金水,回顾建国后广东的两次登革热大流行警惕登革热在我国的再爆发,中国国境卫生检疫杂志,1999,22(4):217-220。
    11.黄健人,茹峰,张高德,傅德坚,陈德贵,方德文。埃及伊蚊的监测,中国媒介生物学及控制杂志,1996,7(6):404-407。
    12.李鹏,陈叶,戴孟阳,黄牧,何秀菊,李清,王萍,沈阳市首例输入性登革热疫情调查处理报告,现代预防医学,2006,33(6):1007-1008。
    13.李世清,何似,陈润,徐保海,许龙善,福建省首次从病人血清及蚊体分离出登革病毒的研究,中国人兽共患病杂志,2000,16(1):55-56。
    14.林立辉,付廷荣,白纹伊蚊对产卵容器的选择,昆虫知识,1984,04:13-14。
    15.林立辉,方美玉,陈翠华,彭翼飞,白纹伊蚊传播登革病毒的媒介效能研究,中国媒介生物学及控制杂志,2000,11(3):173-176。
    16.林立辉,黄兆鹏,白志军,陈唯军,刘建伟,方美玉,广东登革热媒介白纹伊蚊孳生容器类型及其防制效果研究,解放军预防医学杂志,2000,18(4):261-265。
    17.林立辉,李锦清,温卫东,刘建伟,李荣彪,李云,白志军,方美玉,佛山市城区登 革热媒介白纹伊蚊的监测与防治研究,中华卫生杀虫药械,2004,10(6):363-368。
    18.林立丰,卢文成,蔡松武,段金花,易建荣,邓锋,陈清,陈晓光,新型登革热媒介监测诱蚊诱卵器的设计及效果研究,中国媒介生物学及控制杂志,2005,16(1):26-29。
    19.林立丰,段金花,李荣彪,林伟波,蔡松武,卢文成,陈清,李锦清,林宏波,易建荣.现场比较诱蚊诱卵器与传统幼虫监测效果的研究,中国媒介生物学及控制杂志,2006,(06):454-457。
    20.刘素蘭,白纹伊蚊成蚊产卵习性的观察,动物学杂志,1958,2(4):203-206。
    21.刘复生,周昌清,林佩卿,白纹伊蚊种群生态学研究,Ⅴ.广州地区白纹伊蚊自然种群数量季节消长研究中山大学学报(自然科学版),1990,29(2):118-122。
    22.柳忠婉,张跃进;杨亚钊,白纹伊蚊实验种群动态的研究,昆虫学报,1985,28(3):274-281。
    23.罗会明,何剑峰,郑夔,李灵辉,江立敏,广东省1990-2000年登革热流行病学分析,中华流行病学杂志,2002,23(6):427-430。
    24.罗雷,杨智聪,王玉林,刘于飞,秦鹏哲,董智强,沈纪川,李铁刚,康燕,广州市2006年登革热疫情流行病学特征分析,华南预防医学,2007,33(5):11-14。
    25.陆宝麟主编.中国登革热媒介及其防治.贵州人民出版社,1990,12-57。
    26.陆宝麟,吴厚永,主编,中国重要医学昆虫分类与鉴别.河南科学技术出版社,2003。
    27.毛祥华,张再兴,中国登革热的流行现状,中国病原生物学杂志,2007,2(5):385-388。
    28.彭维斌,杨开玺,徐文斌,一起由输入病例引起登革热暴发的流行病学调查,现代预防医学,2007,34(14):2752-2753。
    29.舒莉萍,陈阿英,黄大兴等.贵州省人群登革病毒感染率的调查.贵阳医学院学报,1999,(4):340-341。
    30.舒莉萍,左丽,郝牧,赵星,从贵州白纹伊蚊体内分离到一株2型登革病毒,微生物学报,2004,44(2):153-156。
    31.王夏,罗同勇,周旺,彭劲松,周漩,刘亚民,代生辉,魏善波,武汉地区首次发生输入性登革热疫情的调查,中华流行病学杂志,2004,25(10):897。
    32.王临旭,李羽,张岩,聂青和,白雪帆,贾战生,谢玉梅,康文臻,西安地区输入性登革热3例,西北国防医学杂志,2006,27(2):95-97。
    33.王敬军,王丽,邓勇,余鹏搏,王勤,陕西省调查处理输入性登革热病例的报告,中国热带医学,2007,7(9):1633-1634。
    34.王怀位,王新国,登革热媒介伊蚊的种群监测和防治,医学动物防制,2000,16(7):389-393。
    35.王士珍,徐仁权,徐友祥,任文军,蒋丽亚,胡家官,蔡恩茂,上海地区登革热媒介的现状及孳生习性调查,中国媒介生物学及控制杂志,2003,14(2):124-127。
    36.谢淑云,王臻,杨仕贵等.浙江省一起输入性登革热暴发的流行病学调查分析,疾病监测,2005,20(7):353-355。
    37.徐仁权,蔡恩茂,徐友祥,王士珍,蒋丽亚,刘丽军,任文军,上海地区白纹伊蚊监测与药物防制研究,中国媒介生物学及控制杂志,2003,14(4):256-261。
    38.许龙善,台湾登革热的流行与控制,海峡预防医学杂志,2000,6(1):20-21。
    39.薛瑞德,1987年以来自纹伊蚊的-研究状况及其未来.中国媒介生物学及控制杂志,1994,5(5):392-294。
    40.姚丽君,黄建云,佘焕昭,张旭彬,许璐,廖朝晖,汕头市2006年登革热的流行情况及防制对策,中国热带医学,2007,7(6):895-896。
    41.杨振洲,白纹伊蚊卵滞育的实验观察,昆虫学报,1988,31(3):287-295。
    42.杨芬,罗会明,何剑峰,梁文佳,广东省2006年登革热流行病学分析,华南预防医学,2007,33(5):8-11。
    43.杨佩英,秦鄂德主编.登革热和登革出血热.北京:人民军医出版社,1998,10-20。
    44.严子锵,胡志刚,江毅民,伍浩荣,潘志民,标准间指数在白纹伊蚊自然种群动态监测中的应用研究,中华卫生杀虫药械,2006,12(5):352-355。
    45.严子锵,胡志刚,江毅民,伍浩荣,广州地区白纹伊蚊自然种群幼虫的分布特征,中国媒介生物学及控制杂志,2007,18(3):93-196。
    46.姚若东,孙虹,高乃科,王遇春,曾新宇,珠海口岸登革热传播媒介的调查研究,中国媒介生物学及控制杂志,2006,(02):130-131。
    47.易彬樘,张治英,徐德忠,席云珍,付建国,罗军,袁明辉,刘少群,邝铿,广东省登革热及媒介种群的空间分布,第四军医大学学报,2003,24(17):1623-1626。
    48.赵卫,曹虹,张文炳,登革病毒与登革热的起源研究,中国人兽共患病杂志,2006,22(2):170-171。
    49.赵星,左丽,舒莉萍,白纹伊蚊贵州麻尾株垂直传播登革病毒实验研究,贵阳医学院学报,2004,29(2):95-98。
    50.赵治国,中国登革热控制概述,中国流行病学杂志,2000,21(3):223-224。
    51.张复春,卢业成,陈燕清,王建,陈万山,尹炽标,杨湛,唐小平,2002至2003年广州及周边地区1032例登革热的临床特征,中华传染病杂志,2005, 23(2):121-124。
    52.张金桐,影响昆虫产卵行为的化学因素,寄生虫与医学昆虫学报,1994,1(2):61-67。
    53.张海林,自登云,米竹青,龚振达,施华芳等,云南白纹伊蚊分布特点及与虫媒病毒的关系,中国媒介生物学及控制杂志,2001,12(2):103-105。
    54.张海林,米竹青,张云智,白纹伊蚊和埃及伊蚊经卵传递登革病毒的研究,中国病毒学,1996,11(3):230-236。
    55.张海林,米竹青,张云智,白纹伊蚊和埃及伊蚊对基孔肯雅病毒的易感性和传播性的研究,中国病毒学,1994,9(3):195-200。
    56.张海林,自登云,米竹青,龚正达,施华芳,张云智,侯宗柳,杨兰萍.云南白纹伊蚊分布特点及与虫媒病毒的关系,中国媒介生物学及控制杂志,2001,(02):103-110。
    57.郑能雄,王宗汉,林云钦等.1999-2001年福州市登革热流行病学监测结果分析,现代预防医学,2002,29(4):495-497。
    58.钟作良,何桂铭,不同温度下白纹伊蚊生命生殖力表,昆虫学报,1990,33(2):64-69。
    59.自登云,陈伯权,俞永新.虫媒病毒与虫媒病毒病.第1版.昆明:云南科技出版社,1995。
    60.曾林海,赵伟,王志光,杨霞,李善干.中国热带医学,海南省白纹伊蚊、埃及伊蚊对菊酯类杀虫剂的敏感性测定,2005,(05):1396-1399。
    61.Allan S.A.and Kline D.L.,Evaluation of organic infusions and synthetic compounds mediating oviposition in Aedes albopictus and Aedes aegypti(Diptera:Culicidae),Journal of Chemical Ecology,1995,21(11):1847-1860.
    62.Allan S.A.and Kline D.L.,Larval rearing water and preexisting eggs influence oviposition by Aedes aegypti and Aedes.albopictus(Diptera:Culicidae).J Med Entomol.1998,35(6):943-947.
    63.Armengol G.,Hernandez J.,Velez J.G.,Orduz S.,Long-lasting effects of a Bacillus thuringiensis serovar israelensis experimental tablet formulation for Aedes aegypti (Diptera:Culicidae) control.J Econ Entomol.2006,99(5):1590-1595.
    64.Arredondo-Jimenez J.I.,Valdez-Delgado K.M.,Aedes aegypti pupal/demographic surveys in southern Mexico:consistency and practicality.Ann Trop Med Parasitol.2006;100(Suppll):17-32.
    65.Barbazan P.,Tuntaprasart W.,Souris M.,Demoraes F.,Nitatpattana N.,Boonyuan W.,Gonzalez J.P.,Assessment of a new strategy,based on Aedes aegypti(L.) pupal productivity, for the surveillance and control of dengue transmission in Thailand. Ann Trop Med Parasitol. 200%, 102(2): 161-171.
    66. Barrera R., Amador M, Clark G.G., Use of the pupal survey technique for measuring Aedes aegypti (Diptera: Culicidae) productivity in Puerto Rico. Am J Trop Med Hyg. 2006;74(2): 290-302.
    67. Barrera R., Amador M., Clark G.G., Ecological factors influencing Aedes aegypti (Diptera: Culicidae) productivity in artificial containers in Salinas, Puerto Rico. J Med Entomol. 2006;43(3): 484-492.
    68. Benzon G.L. and Apperson C.S., Reexamination of chemically mediated oviposition behavior in Aedes aegypti (L)(Diptera:Culicidae), J Med Entomol, 1998, 25(3): 158-164.
    69. Bellini R., Carrieri M., Burgio G., Bacchi M., Efficacy of different ovitraps and binomial sampling in Aedes albopictus surveillance activity. J Am Mosq Control Assoc. 1996 , 12(4): 632-636.
    70. Bellini R., Carrieri M., Bacchi M., Fonti P., andCelli G., Possible utilization of metallic copper to inhibit Aedes albopictus (Skuse) larval development. JAMCA,1998,14: 451-456.
    71. Brito M, Forattini O.P., Epub 2004 Apr 26. Productivity of Aedes albopictus' breeding containers in Paraiba Valley, Brazil, Rev Saude Publica. 2004 , 38(2): 209-215.
    72. Burkett D.A., Kelly R., Porter C.H., and Wirtz R.A., Commercial mosquito trap and gravid trap oviposition media evaluation, Atlanta, Georgia. J Am Mosq Control Assoc, 2004, 20(3): 233-238.
    73. Cabrera-Batista B., Skewes-Ramm R., Fermin C.D., Garry R.F., Dengue in the Dominican Republic: epidemiology for 2004. Microsc Res Tech. 2005 , 68(3-4): 250-254.
    74. Chadee D.D., Corbet P.S., Talbot H., Proportions of eggs laid by Aedes aegypti on different substrates within an ovitrap in Trinidad, West Indies. Med Vet Entomol. 1995, 9(1): 66-70.
    75. Chadee D.D., Key premises, a guide to Aedes aegypti (Diptera: Culicidae) surveillance and control. Bull Entomol Res. 2004, 94(3): 201-207.
    76. Chadee D.D. and Corbet P.S., Diel Pattern of oviposition in the laboratory of the mosquito Aedes albopictus (Skuse) (Diptera: Culicidae). Ann Trop Med Parasitol. 1989, 83(4): 423-429.
    77. Chadee D.D. and Corbet P.S., The gonotrophic status and diel pattern of entry to outdoor oviposition sites of female Aedes aegypti (L.) (Diptera: Culicidae), Ann Trop Med Parasitol. 1993, 87(3): 263-268.
    
    78. Chadee D.D., Lakhan A., Ramdath W.R., Persad R.C.,Oviposition response of Aedes aegypti mosquitoes to different concentrations of hay infusion in Trinidad, West Indies. J Am Mosq Control Assoc. 1993, 9(3): 346-348.
    
    79. Clements, W. H., Cherry D. S. and Cairns J. Structural alterations in aquatic insects communities exposed to copper in laboratory streams. Environ. Toxicol. Chem . 1988, 84: 715-722.
    
    
    80. Chen Chee Dhangl, Seleena Benjaminl, Mohd. Masri Saranuml, et al,Dengue vector surveillance in urban residential and settlement areas in Selangor, Malaysia, Tropical Biomedicine ,2005, 22(1): 39-43.
    
    81. Claudia M. E., Romero-vivas K. I., Andrew et al. Investigation of relations between aedes aegypti egg,larvae,pupae,and adult density indices where their main breeding sites were located indoors. J Am Mosq Control Assoc, 2005, 21(1): 15-21.
    
    82. Corbet P.S. and Chadee D.D., The diel pattern of entry to outdoor oviposition sites by female Aedes aegypti (L.) (Diptera: Culicidae). Ann Trop Med Parasitol. 1992, 86(5): 523-528.
    
    83. Comiskey N., Wesson D. M., Dirofilaria (Filarioidea: Onchocercidae) infection in Aedes albopictus (Diptera: Culicidae) collected in Louisiana. J. Med. Entomol. 1995, 32(5): 734-737.
    
    84. Dennett J.A., Vessey N.Y., Parsons R.E., A comparision of seven traps used for collection of Aedes albopictus and Aedes aegypti originating from a large tire repository in Harris County (Houston), Texas. J Am Mosq Control Assoc. 2004 , 20(4): 342-349.
    
    85. Delia Torre, A., Raineri V. and Cancrini G., Effettodel rame metallico sullo sviluppo larvale di Aedes albopictus:priml dati di laboratorio. Parassitologia 1993,35: 51-53.
    
    86. Facchinelli. L., Valerrio L., Pombi M. , et al. Development of a novel sticky trap for container-breeding mosquitoes and evaluation of its sampling properties to monitor urban populations of Aedes albopictus. Med Vet Entomol, 2007,21: 183-195.
    
    87. Fay R.W., Eliason D.A., A preferred oviposition site as surveillance method for Aedes aegypti. Mosq News ,1966, 26: 531-535.
    
    88. Fay, Richard W. and William H., Prince. A modified visual trap for Aedes aegypti.Mosquito News,1970, 30: 20-23.
    89. Favier C., Degallier N., Vilarinhos P. T., de Carvalho Mdo S, Yoshizawa M.A., Knox . M.B., Effects of climate and different management strategies on Aedes aegypti breeding sites: a longitudinal survey in Brasilia (DF, Brazil). Trop Med Int Health. 2006,11(7):1104-1118
    
    90. Focks D.A., Chadee D.D., Pupal survey: an epidemiologically significant surveillance method for Aedes aegypti: an example using data from Trinidad. Am J Trop Med Hyg. 1997,56(2): 159-167.
    
    91. Francy D. B., Karabatsos N., Wesson D. M. , et al. A new arbovirus from Aedes albopictus, an asian mosquito established in the United States. Science. 1990, 250: 1738-1740.
    
    92. Freier, J. E. and Francy D. B., A duplex cone trap for the collection of adult Aedes albopictus. J. Am. Mosq. Control Assoc. 1991, 7: 73-79.
    
    93. Gama R.A., Silva E.M., Silva I.M., Resende M.C., Eiras A.E., Evaluation of the sticky MosquiTRAP for detecting Aedes (Stegomyia) aegypti (L.) (Diptera: Culicidae) during the dry season in Belo Horizonte, Minas Gerais, Brazil. Neotrop Entomol. 2007, 36(2): 294-302.
    
    94. Gould R., Old tyres don't die, they just dissolve away. New Scientist Technology, 1994, 12: 19.
    
    95. Gratz N.G., Critical review of the vector status of Ae. albopictus. Med Vet Entomol, 2004,18:215-217.
    
    96. Gubler D.J., Dengue/dengue haemorrhagic fever: history and current status. Novartis Found Symp. 2006, 277: 3-16;
    
    97. Goh K.T., Dengue-a re-emerging infectious disease in Singapore. Ann Acad Med Singapore. 1997, 26(5): 664-670.
    
    98. Guzman M.G., Alvarez M., Rodriguez R., Rosario D., Vazquez S., Vald s L., Cabrera M.V., Kouri G., Fatal dengue hemorrhagic fever in Cuba, 1997. Int J Infect Dis. 1999, 3(3): 130-135.
    
    99. Gupta E., Dar L., Kapoor G., Broor S. , The changing epidemiology of dengue in Delhi, India. Virol, J. 2006 , 5: 83-92.
    
    100.Halstead S.B., The XXth century dengue pandemic: need for surveillance and research. World Health Stat Q. 1992, 45(2-3): 292-298.
    101.Hare L., Aquatic insect and trace metals: Bioavailability,bioaccumulation, and toxicity. Crit. Rev. Toxicol. 1992, 22: 327-369.
    102.Hoel D.F., Kline D.L., Allan S.A., Grant A. Evaluation of carbon dioxide, 1-octen-3-ol, and lactic acid as baits in Mosquito Magnet Pro traps for Aedes albopictus in north central Florida. J Am Mosq Control Assoc. 2007; 23(1): 11-17.
    103.Holick J., Kyle A., Ferraro W. , et al. Discovery of Aedes albopictus infected with West Nile virus in southeastern Pennsylvania. J. Am. Mosq. Control. Assoc. 2002, 18(2): 131.
    104.Huang J.H., Liao T.L., Chang S.F., Su C.L., Chien L.J., Kuo Y.C., Yang C.F., Lin C.C., Shu P.Y., 2007, Laboratory-based Dengue Surveillance in Taiwan, 2005: A Molecular Epidemiologic Study. Am J Trop Med Hyg. Nov;77(5): 903-909.
    105.Isoe J., Millar J.G., and Beehler J.W., Bioassays for Culex (Diptera: Culicidae) Mosquito Oviposition Attractants and Stimulants, J Med Entomol. 1995, 32(4): 475-483.
    106.Isoe, J., Millar, J.G., Characterization of factors mediating oviposition site choice by Culex tarsalis. J Am Mosq Control Assoc,1995,11(1): 21-28.
    107.Jensen, T., Willis O.R., Fukuda T., and Barnard D. R. Comparison of Bi-directional Fay, Omnidirectional,CDC, and duplex cone traps for sampling adult Aedes albopictus and Aedes aegypti in north Florida. J. Am. Mosq. Control Assoc. 1994,10(1): 74-78.
    108.Jones J.W., Sithiprasasna R., Schleich S., Coleman R.E., Evaluation of selected traps as tools for conducting surveillance for adult Aedes aegypti in Thailand. J Am Mosq Control Assoc. 2003, 19(2): 148-150.
    109.Kay B.H., Barker-Hudson, P., Hapgood, G.D., McCurley, J.O., Lyons, G.C., and Ives W, Aedes aegypti and dengue in the Townsville area, 1982-1985. Gen Appl Entomol, 1987,19:2-10.
    110.Kay B.H., Sutton K.A., and Russell B.M., A sticky entry-exit for sampling mosquit oes in subterranean habitats, J Am Mosq Control Assoc, 2000, 16(3): 262-265.
    111.Knight K. L., Stone A., A Catalogue of the Mosquitoes of the World, 2nd, The Thomas Say Foundation, 1977, 161: 156.
    112.Knox T.B., Yen N.T., Nam V.S., Gatton M.L., Kay B.H., Ryan P.A., Critical evaluation of quantitative sampling methods for Aedes aegypti (Diptera: Culicidae) immatures in water storage containers in Vietnam. J Med Entomol. 2007 , 44(2): 192-204.
    113.Knudsen A.B. Global distribution and continuing spread of Aedes albopictus. Parassitologia. 1995, 37(2-3): 91-97.
    114.Krockel U., Rose A., Eiras A.E., Geier, New tools for surveillance of adult yellow fever mosquitoes: comparison of trap catches with human landing rates in an urban environment. J Am Mosq Control Assoc. 2006 Jun;22(2):229-38.
    
    115.Koenraadt C.J., Jones J.W., Sithiprasasna R., Scott T.W., Standardizing container classification for immature Aedes aegypti surveillance in Kamphaeng Phet, Thailand. J Med Entomol. 2007 ,44(6): 938-944.
    116.Lampman, R. L. and Novak. R. J., Attraction of Aedes albopictus adults to sod infusion, J.Am.Mosq.Control Assoc, 1996, 12: 119-124.
    
    117.Lee M.S., Hwang K.P., Chen T.C., Lu P.L., Chen T.P., Clinical characteristics of dengue and dengue hemorrhagic fever in a medical center of southern Taiwan during the 2002 epidemic. J Microbiol Immunol Infect. 2006, 39(2): 121-129.
    118.Lenhart A.E., Castillo C.E., Oviedo M., Villegas E. Use of the pupal/demographic-survey technique to identify the epidemiologically important types of containers producing Aedes aegypti (L.) in a dengue-endemic area of Venezuela. Ann Trop Med Parasitol. 2006, 100 (Suppll): 53-59.
    
    119.Mahilum M.M., Ludwig M, Madon M.B., Becker N. Evaluation of the present dengue situation and control strategies against Aedes aegypti in Cebu City, Philippines. J Vector Ecol. 2005, 30(2): 277-283.
    
    120.Marques C.C., Marques G.R., de Brito M, dos Santos Neto L.G., Ishibashi Vde C, Gomes Fde A. Comparative study of larval and ovitrap efficacy for surveillance of dengue and yellow fever vectors, Rev Saude Publica. 1993, 27(4): 237-241.
    121.Medlock J.M., Avenell D., Barrass I., Leach S., Analysis of the potential for survival and seasonal activity of Aedes albopictus (Diptera: Culicidae) in the United Kingdom. J Vector Ecol. 2006, 31(2): 292-304.
    
    122.Miller B. R., Ballinger M. E.. Aedes albopictus mosquitoes introduced into Brazil: vector competence for yellow fever and dengue viruses. Trans. R.Soc. Trop. Med. Hyg. 1988, 82:476-477.
    
    123.Mitchell C. J. and D. J. Gubler. Vector competence of geographic strains of Aedes albopictus and Aedes pilynesiensis and certain other Aedes mosquitos for Ross River Virus. J. Am. Mosq. Control. Assoc. 1987, 3(2): 142-147.
    
    124.Mogi M., Khamboonruang C., Choochote W., Suwanpanit P. Ovitrap surveys of dengue vector mosquitoes in Chiang Mai, northern Thailand: seasonal shifts in relative abundance of Aedes albopictus and Aedes. aegypti. Med Vet Entomol. 1988 , 2(4): 319-324.
    125.Moore C.G.,Francy D.B.,Eliason D.A.,Monath T.P.,Aedes albopictus in the United States:rapid spread of a potential disease vector.J Am Mosq Control Assoc.1988,4(3):356-361.
    126.Moore C.G.and Mitchell C.J.,Aedes albopictus in the United States:ten-year presence and public health implications.Emerg.Infect.Diseases,1997,3:329-334。
    127.Morato V.C.,Teixeira Mda G,Gomes A.C.,Bergamaschi D.P.,Barreto M.L.,Infestation of Aedes aegypti estimated by oviposition traps in Brazil.Rev Saude Publica.2005,39(4):553-558.
    128.Muri L.E.,Kay B.H.Aedes aegypti survival and disperal estimated by mark-release-recapture in northern Australia.Am J Trop Med Hyg,1998,58:277-282.
    129.Nam V.S.,Ryan P.A.,Yen N.T.,Phong T.V.,Marchand R.P.,Kay B.H.,Quantitative evaluation of funnel traps for sampling immature Aedes aegypti from water storage jars.J Am Mosq Control Assoc.2003,19(3):220-227.
    130.Nogueira R.M.,de Araujo JM,Schatzmayr H.G.Dengue viruses in Brazil,1986-2006.Rev Panam Salud Publica.2007,22(5):358-363.
    131.Nogueira L.A.,Gushi L.T.,Miranda J.E.,Madeira N.G.,Ribolla P.E.Application of an alternative Aedes species(Diptera:culicidae) surveillance method in Botucatu City,Sao Paulo,Brazil.Am J Trop Med Hyg.2005,73(2):309-311.
    132.Ordonez-Gonzalez J.G.,Mercado-Hernandez R.,Flores-Suarez A.E.,et al,the use of sticky ovitraps to estimate dispersal of Aedes aegypti in northeastern Mexico,J Am Mosq Control Assoc.2001,17(2):93-97.
    133.O'Meara,G.F.,Evans L.F.,andGettman A.D..Reduced mosquito production in cemetery vases with copper lines.JAMCA,1992a,8:419-420.
    134.O'Meara,G.F.,Gettman A.D.,Evans.L.F.,and Scheel F.D..Invasion of cemeteries in Florida by Aedes albopictus.JAMCA,1992b.8:1-10.
    135.Ooi E.E.,Goh K.T.,Gubler D.J.887-93Dengue prevention and 35 years of vector control in Singapore.Emerg Infect Dis.2006,12(6):1147-1153.
    136.Perich M.J.,Kardec A.,Braga I.A.,Portal I.F.,Burge R.,Zeichner B.C.,Brogdon W.A.,Wirtz R.A.Field evaluation of a lethal ovitrap against dengue vectors in Brazil.Med Vet Entomol.2003,17(2):205-210.
    137.Pinheiro F.P.,Corber S.J.Global situation of dengue and dengue haemorrhagic fever,and its emergence in the Americas.World Health Stat Q.1997,50(3-4):161-169.
    138.Quails W.A., Mullen G.R., Evaluation of the Mosquito Magnet Pro trap with and without 1-octen-3-ol for collecting Aedes albopictus and other urban mosquitoes. J Am Mosq Control Assoc. 2007, 23(2): 131-136.
    139.Raineri, V., F. Rongioletti, and A. Rebora.Osservazioni sulla presenza di Aedes albopictus in Liguria. Parassitologia,1993, 35: 31-32.
    140.Raineri, V., G. Trovato, A. Sabatini, and M. Coluzzi.Ulteriori dati sulla diffusione a Genova di Aedes albopictus. Parassitologia ,1991, 33: 183-185.
    
    141.Rayms-Keller, A., Olson K. E., McGraw M., Oray C., Carlson J. O, and Beaty B. J.. Effect of heavy metals on Aedes aegypti (Diptera:Culicidae) larvae. Ecotoxicol. Environ.Saf. 1998, 39: 41-47.
    142.Reiter, Paul. A portable, battery powered trap for collecting gravid Culex mosquitoes. Mosquito News, 1983,43:496 498.
    
    143.Reiter, P., Amador M. A. and Colon, N., Enhancement of the CDC ovitrap with hay infusion for daily monitoring of Aedes aegypti populations. J Am Mosq Control Assoc, 1991,7:52-55.
    144.Reiter P. Aedes albopictus and the world trade in used tires, 1988-1995: the shape of things to come? J. Am. Mosq. Control. Assoc. 1998,14(1):83-94.
    145.Rodhain F. Aedes albopictus: a potential problem in France. Parassitologia. 1995 Dec;37(2-3):115-119.
    146.Romi R. History and updating on the spread of Aedes albopictus in Italy. Parassitologia. 1995, 37(2-3): 99-103.
    147.Ritchie, S. A., Hay infusion and iospropyl alcohol-baited CDC light trap; a simple effective trap for gravid Culex mosquitoes. Mosq.News,1984, 44: 404-407.
    148.Ritchie S.A., Long S., Hart A., et al , An adultcidal sticky ovitrap for sampling container-breeding mosquitoes, Journal of the American Mosquito Control assocition,2003,19(3):235-242.
    
    149.Ritchie S.A., Long, S., Smith, G., Pyke, A., Knox, T.B., Entomological investigations in a focus of dengue transmission in Cairns, Queensland, Australia, by using the sticky ovitraps. J Med Entomol. 2004,41(1): 1-4.
    
    150.Ritchie S.A., Moore P., Carruthers M., Williams C., Montgomery B., Foley P., Ahboo S, van den Hurk A.F., Lindsay M.D., Cooper B, Beebe N, Russell R.C. Discovery of a widespread infestation of Aedes albopictus in the Torres Strait, Australia, J Am Mosq Control Assoc. 2006, 22(3): 358-365.
    151.Romero-Vivas C.M., Wheeler J.G., Falconar A.K., An inexpensive intervention for the control of larval Aedes aegypti assessed by an improved method of surveillance and analysis. J Am Mosq Control Assoc. 2002, 18(1): 40-46.
    152.Romero-Vivas C.M., Arango-Padilla P., Falconar A.K., Pupal-productivity surveys to identify the key container habitats of Aedes aegypti (L.) in Barranquilla, the principal seaport of Colombia. Ann Trop Med Parasitol. 2006, 100(Suppll): 87-95.
    153.Romero-Vivas C.M., Llinas H., Falconar A.K., Three calibration factors, applied to a rapid sweeping method, can accurately estimate Aedes aegypti (Diptera: Culicidae) pupal numbers in large water-storage containers at all temperatures at which dengue virus transmission occurs. J Med Entomol. 2007, 44(6): 930-937.
    154.Russell R.C. and Ritchie S.A., Surveillance and behavioral investigation of Aedes. albopictus and Aedes polynesiensis in Moorea, French Polynesia, using a sticky ovitrap, J Am Mosq Control Assoc , 2004, 20(4): 370-375.
    155.Russell R.C., Williams C.R., Sutherst R.W., Ritchie S.A. Aedes (Stegomyia) albopictus--a dengue threat for southern Australia? Commun Dis Intell. 2005, 29(3): 296-298.
    156.Santana A.L., Roque R.A., Eiras A.E., Characteristics of grass infusions as oviposition attractants to Aedes (Stegomyia) (Diptera: Culicidae). J Med Entomol. 2006, 43(2): 214-220.
    157.Savage H. M., Niebylski M. L., Smith G. C., et al. Host-feeding patterns of Aedes albopictus at temperate N.A site. J. Med. Entomol. 1993, 30: 27-34.
    158.Setha T., Chantha N., Socheat D. Efficacy of Bacillus thuringiensis israelensis, VectoBac WG and DT, formulations against dengue mosquito vectors in cement potable water jars in Cambodia. Southeast Asian J Trop Med Public Health. 2007 , 38(2): 261-268.
    159.Shroyer D. A. Aedes albopictus and arboviruses: a concise review of the literature. J. Am. Mosq. Control. Assoc.1986, 2(4): 424-428.
    160.Sithiprasasna R., Mahapibul P., Noigamol C., Perich M.J., Zeichner B.C., Burge B., Norris S.L., Jones J.W., Schleich S.S., Coleman R.E., Field evaluation of a lethal ovitrap for the control of Aedes aegypti (Diptera: Culicidae) in Thailand. J Med Entomol. 2003, 40(4): 455-462.
    
    161.Singh N., Kiedrzynski T, Lepers C., Benyon E.K. Dengue in the Pacific-an update of the current situation. Pac Health Dialog. 2005, 12(2):111-119.
    162.Sumarmo . Dengue haemorrhagic fever in Indonesia. Southeast Asian , J Trop Med Public Health. 1987, 18(3): 269-274.
    
    163.Sulaiman S., Pawanchee Z.A., Arifin Z., Wahab A. Relationship between Breteau and House indices and cases of dengue/dengue hemorrhagic fever in Kuala Lumpur, Malaysia. J Am Mosq Control Assoc. 1996, 12(3 Pt 1): 494-496.
    
    164.Thavara, U., Tawatsin, A., Chompoosri, J., Evaluation of attractants and egg-laying substrate preference for oviposition by Aedes albopictus (Diptera: Culicidae). J Vector Ecol. 2004, 29(1): 66-72.
    
    165.Toma L., Severini F., Di Luca M., Bella A., Romi R., Seasonal patterns of oviposition and egg hatching rate of Aedes albopictus in Rome. J Am Mosq Control Assoc. 2003, 19(1): 19-22.
    
    166.Trexler J.D., Apperson C.S., Schal C., Diel oviposition patterns of Aedes albopictus (Skuse) and Aedes triseriatus (Say) in the laboratory and the field. J Vector Ecol.1997, 22(1): 64-70.
    
    167.Trexler J.D., Apperson C.S., Schal C., Laboratory and field evaluations of oviposition responses of Aedes albopictus and Aedes triseriatus (Diptera: Culicidae) to oak leaf infusions. J Med Entomol. 1998, 35(6): 967-976.
    
    168.Trexler J.D., Apperson C.S., Gemeno C., Perich M.J., Carlson D., Schal C., Fi eld and laboratory evaluations of potential oviposition attractants for Aedes alb opictus (Diptera: Culicidae). J Am Mosq Control Assoc. 2003a, 19(3): 228-234.
    169.Trexler J.D., Apperson C.S., Zurek L., Gemeno C., Schal C., Kaufman M., Walker E., Watson D.W., Wallace L. Role of bacteria in mediating the oviposition responses of Aedes albopictus (Diptera: Culicidae). J Med Entomol. 2003b, 40(6): 841-848.
    170.Tun-Lin W, Kay B.H., Barnes A. Understanding productivity, a key to Aedes aegypti surveillance. Am J Trop Med Hyg. 1995, 53(6): 595-601.
    171.Tun-Lin W, Kay B.H., Barnes, The Premise Condition Index: a tool for streamlining surveys of Aedes aegypti. Am J Trop Med Hyg. 1995, 53(6): 591-594.
    172.Williams C.R., Long S.A., Russell R.C., Ritchie S.A. Field efficacy of the BG-Sentinel compared with CDC Backpack Aspirators and CO_2-baited EVS traps for collection of adult Aedes aegypti in Cairns, Queensland, Australia. J Am Mosq Control Assoc. 2006, 22(2): 296-300.
    
    173.Williams C.R., Long S.A., Russell R.C., Ritchie S.A. Optimizing ovitrap use for Aedes aegypti in Cairns, Queensland, Australia: effects of some abiotic factors on field efficacy. J Am Mosq Control Assoc. 2006, 22(4): 635-640.
    174. Williams, C.R., Ritchie, S.A., Long, S.A., Dennison, N., Russell, R.C., Impact of a bifenthrin-treated lethal ovitrap on Aedes aegypti oviposition and mortality in north Queensland, Australia. J Med Entomol. 2007, 44(2): 256-262.
    175.Wilton D. P., Preliminary evaluation of a black cylinder suction trap for Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae). J. Med. Entomol..1985, 22: 113-114.
    176.Yap H.H., Lee C.Y., Chong N.L., Foo A.E., Lim M.P., Oviposition site preference of Aedes albopictus in the laboratory. J Am Mosq Control Assoc. 1995, 11(1): 128-132.
    177.Zeichner B.C., Perich M.J., Laboratory testing of a lethal ovitrap for Aedes aegypti. Med Vet Entomol. 1999, 13(3): 234-238.
    178.Zhang L.Y. and Lei C.L., Evaluation of sticky ovitraps for the surveillance of Aedes (Stegomyia) albopictus (Skuse) and the screening of oviposition attractants from organic infusions, Ann Trop Med Parasitol. 2008, 102(5): 399-407.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700