云南切梢小蠹对云南松树干和枝梢挥发性物质趋向反应的差异分析

利用GC-MS联用仪和计算机信息检索法,通过对云南松Pinus yunnanensis树干韧皮部和枝梢的挥发性物质成分的分析发现,二部位所含挥发性物质在组成成分和含量上存在明显差异.云南松树干挥发物以α-蒎烯为主,含量达81.01%,枝梢为挥发物以α-蒎烯和β-水芹烯为主,含量分别达29.20%和30.52%.与云南松...     

云南切梢小蠹对云南松树的蛀干危害及致死机理

蛀干危害是云南切梢小蠹致死云南松树的关键环节。通过控制云南切梢小蠹蛀干密度,对云南切梢小蠹在自然条件下蛀干行为与危害进行了首次探讨。结果表明,云南切梢小蠹蛀干密度与云南松存活率呈负相关,蛀干密度直接决定云南松死亡或存活。研究发现,蛀干密度115坑/m2是云南松树的最低致死密度阈值,云南松树在蛀干密度低于26.4坑/m2情况下存活,在26.4-115坑/m2有部分存活,超过115坑/m2以后将被害致死。云南切梢小蠹对树干攻击形成有卵和无卵两类坑道。形成无卵坑道的蛀干攻击可导致树势衰弱,形成有卵坑道的蛀干危害严重破坏了韧皮组织,是导致云南松死亡的直接原因。     

云南横坑切梢小蠹生物学研究

横坑切梢小蠹Tomicus minor (Hartig)是云南松Pinus yunnanensis Franchet的主要次期性害虫之一。1980年以来,该虫与纵坑切梢小蠹T. piniperda（L.）一起在中国西南部大量发生,导致数十万公顷云南松林受害。本文报道了横坑切梢小蠹在云南地区的生活史、生长、发育、繁殖等生物学特征。横坑切梢小蠹年生活史为一代,前后两代在冬春季有部分重叠。成虫羽化于4月下旬开始陆续,5 月下旬结束。成虫羽化后即飞到树冠上蛀食枝梢,直到11月发育成熟,开始繁殖。在此期间,每头成虫可以蛀食4～6个枝梢。横坑切梢小蠹在云南没有越冬习性。繁殖期从11月至次年3月。成虫主要在已经受到纵坑切梢小蠹危害的树木的中、下部产卵。繁殖期较纵坑切梢小蠹约迟1周。由于横坑切梢小蠹从枝梢到树干对云南松持续危害,对树木的危害性较在其它地区更为严重。横坑切梢小蠹利用受到纵坑切梢小蠹蛀害的树木繁殖产卵,加强了蠹虫对云南松树的危害,加速了受害树木的死亡进程。横坑切梢小蠹的上述生物生态学特征是该虫对云南松造成严重危害的重要原因。从横坑切梢小蠹虫体和虫坑中检测到伴生真菌云南半帚孢Leptographium yunnanensis。横坑切梢小蠹对该菌的带菌率在蛀梢期为11.5%;在蛀干中期约为10%～26%。     

纵坑切梢小蠹携带云南半帚孢研究

云南半帚孢 (Leptogramphyunnanensis)是纵坑切梢小蠹Tomicuspiniperda重要的共生真菌 ,在纵坑切梢小蠹危害寄主树木过程中发挥着重要作用。研究揭示 ,纵坑切梢小蠹主要通过与受到感染云南半帚孢的韧皮组织的接触携带上云南半帚孢的。纵坑切梢小蠹卵、幼虫和蛹对云南半帚孢的带菌率较高 ,均大于 90 % ,而成虫的带菌率较低。纵坑切梢小蠹的体表和体内均携带有云南半帚孢 ,但体表带菌是纵坑切梢小蠹带菌的主要途径。通过对纵坑切梢小蠹成虫头、足、翅和腹部带菌率的研究发现 ,云南半帚孢在纵坑切梢小蠹各部位的分布大体相同 ,揭示纵坑切梢小蠹没有携带云南半帚孢的特化构造或器官。     

光照、温度对纵坑切梢小蠹起飞行为的影响

纵坑切梢小蠹有明显的趋光性。在光照为 1～ 4 0 0 lx范围内 ,趋光性随光照强度提高而增强。完全黑暗条件下 ,蠹虫起飞量极少。在光照 10 0 0 lx,温度 2 5℃下 ,蠹虫起飞率达 77.7%。研究认为 ,温度和光照是纵坑切梢小蠹起飞的重要环境因素     

纵坑切梢小蠹对云南松枝梢提取物趋性测试

纵坑切梢小蠹ＴｏｍｉｃｕｓｐｉｎｉｐｅｒｄａＬ .是松科树木的蛀食性害虫。在过去近 2 0多年中 ,该虫已毁灭云南松林 2 0余万ｈｍ2 ,成为目前云南森林的第一大虫害[1] 。在云南 ,纵坑切梢小蠹常年在云南松 (Ｐｉ ｎｕｓｙｕｎｎａｎｅｎｓｉｓ)枝梢内或树皮下蛀食生活 ,活动     

纵坑切梢小蠹蛀梢期生物学研究

本文研究了纵坑切梢小蠹Tomiaus piniperda对云南松枝梢的危害,并对该虫在蛀梢期的有关生物学特性,如性比、交配、食物选择、卵巢发育、越冬等进行了探讨。在昆明地区,蛀梢期从当年5月持续到次年3月。在此期间,该虫平均可蛀害3-6个枝梢。受害梢以当年生枝梢为主,平均直径为7-8.5mm。同一枝梢可受到多次蛀害。侵入孔距枝梢末端约3～4cm。该虫在蛀梢期已开始交配活动。交配率随卵巢发育进度而增大。各虫态受冬季气温低的影响发育减缓,但均能顺利越冬。     

纵坑切梢小蠹蛀梢期空间分布

在昆明地区,纵坑切梢小蠹（Ｔｏｍｉｃｕｓ　ｐｉｎｉｐｅｒｄａ）成虫蛀梢多集中在蛀干木附近。种群密度以蛀干木为中心向周围是指数递减,散布半径约３０ｍ。在蛀虹梢过程中,该种群逐渐向新区扩张。在树冠内,纵坑切梢小蠹主要分布在４—１０轮枝上。第７轮技虫口百分率最高。６—７轮枝受害率最大。树冠上层受害较其下属于重。从树冠水平层次考察,树冠外层虫量相对集中,约为树冠中、内层虫量之和。树冠内层虫量最少。纵坑切梢小蠹在树冠内的种群分布系由梢径、种群密度、蛀梢行为、降落方式、光照等因素综合影响的结果。     

纵坑切梢小蠹蛀梢期空间分布

在昆明地区,纵坑切梢小蠹(Tomicus piniperda)成虫蛀梢多集中在蛀干木附近。 种群密度以蛀干木为中心向周围呈指数递减,散布半径约30m。在蛀梢过程中,该种群逐渐向新区扩张。在树冠内,纵坑切梢小蠹主要分布在4-10轮枝上。第7轮枝虫口百分率最高。6-7轮枝受害率最大。 树冠上层受害较其下层严重。从树冠水平层次考察,树冠外层虫量相对集中,约为树冠中、内层虫量之和。 树冠内层虫量最少。纵坑切梢小蠹在树冠内的种群分布系由梢径、种群密度、蛀梢行为、降落方式、光照等因素综合影响的结果。     

纵坑切梢小蠹对云南松蛀害研究

在昆明地区,纵坑切梢小蠹Tomicus piniperda L.表现出枝梢聚集、树干蛀害等重要的行为学特征,形成三种基本蛀害模式。横坑切梢小蠹、蓝色伴生真菌参与了纵坑切梢小蠹危害过程,并在其中发挥积极作用。上述因素的综合影响,加强了纵坑切梢小蠹对云南松Pinus yunnanensis寄主树木的危害能力。     

植物挥发性物质在蚜虫寄主定位中的作用

本文综述了植物挥发性物质的化学性质、研究方法及其在蚜虫寄主定位中的作用     

n-Hexanal and (Z)-3-hexenal are generated from arachidonic acid and linolenic acid by a lipoxygenase in Marchantia polymorpha L.

Most terrestrial plants form green leaf volatiles (GLVs), which are mainly composed of six-carbon (C6) compounds. In our effort to study the distribution of the ability of lipoxygenase (LOX) to form GLVs, we found that a liverwort, Marchantia polymorpha, formed n-hexanal and (Z)-3-hexenal. Some LOXs execute a secondary reaction to form short chain volatiles. One of the LOXs from M. polymorpha (MpLOX7) oxygenized arachidonic and α-linolenic acids at almost equivalent efficiency and formed C6-aldehydes during its catalysis; these are likely formed from hydroperoxides of arachidonic and α-linolenic acids, with a cleavage of the bond between carbon at the base of the hydroperoxy group and carbon of double bond, which is energetically unfavorable. These lines of evidence suggest that one of the LOXs in liverwort employs an unprecedented reaction to form C6 aldehydes as by-products of its reaction with fatty acid substrates.     

Response of the pine engraver, Ips pini (Say) (Coleoptera: Scolytidae), to conophthorin and other angiosperm bark volatiles in the avoidance of non-hosts

1 Seventeen non‐host angiosperm bark volatiles, seven of which are antennally active to Ips pini (Say), the pine engraver (PE), were tested for their ability to disrupt the response of the PE to pheromone‐baited traps. 2 Four green leaf volatiles (GLVs) were tested [1‐hexanol (Z)‐3‐hexen‐1‐ol, hexanal, and (E)‐2‐hexenal]. None had any disruptive effect singly, as a group or in all possible blends based on functional groups, despite the fact that the two aldehydes were antennally active. These compounds may have, in some instances, actually masked the disruptive effect of other compounds. The PE thus differs in its response from other Scolytidae, including other Ips spp. 3 Eight non‐host volatiles that were antennally active to other bark beetles, but not to PEs, had no disruptive effect, validating the use of coupled gas chromatographic‐electroantennographic detection analyses to detect compounds with potential behavioural activity. 4 The bicyclic spiroacetal conophthorin, (E)‐7‐methyl‐1,6‐dioxaspiro[4.5]decane, was disruptive when tested alone. When blends of two aldehydes [salicylaldehyde and nonanal] plus an alcohol and a phenol [benzyl alcohol and guaiacol] were combined with conophthorin, an enhanced disruptive effect was revealed. No single compound, other than conophthorin, disrupted the pheromone‐positive response and no blend that did not contain conophthorin was consistently disruptive to both sexes. Conophthorin seems to be a critical component in the non‐host angiosperm message for I. pini during its host selection phase. 5 Combination of the repellent synomones, verbenone and ipsenol, with the five disruptive non‐host volatiles may provide a potent treatment to protect trees, logs or stands from attack by the PE.     

寄主挥发物、叶色和表皮毛在美洲斑潜蝇寄主选择中的作用

在室内条件下 ,初步研究了寄主挥发物、叶色和表皮毛在美洲斑潜蝇寄主选择中的作用。在嗅觉仪试验中 ,寄主叶片挥发物对美洲斑潜蝇雌成虫没有明显的引诱作用 ;在叶色反应试验中 ,美洲斑潜蝇雌成虫在叶子圆片上停留的时间明显大于在滤纸圆片上停留的时间 (p<0 .0 1) ,其在有叶片区域分布的数量明显多于空白对照 (p <0 .0 1) ;在表皮毛试验中 ,美洲斑潜蝇在无毛叶片上的产卵量明显大于在有毛叶片上的产卵量 (p <0 .0 1)。上述结果表明 ,在对寄主的定向和定位过程中 ,美洲斑潜蝇的视觉起着重要的作用 ,而嗅觉不起作用 ;叶片表皮毛有抑制产卵的作用