Occurrence and life-history of Eucryptorrhynchus chinensis in Lingwu, Ningxia

系统调查沟眶象Eucrypt1orrhynchm chinensis(Olivier)在宁夏灵武市的发生情况和特点发现:沟眶象以成虫和幼虫在土壤中越冬,成虫有2个发生高峰期,越冬结束后以成虫越冬的沟眶象出土出现第1个高峰期,以幼虫越冬的沟眶象经化蛹羽化出土出现第2个高峰期;幼虫危害臭椿根部形成的瘤状物可以作为鉴别沟眶象危害的特征;沟眶象幼虫在土壤中垂直分布范围集中在0～45cm深土层,约占80％;成虫出土孔集中在距臭椿树干基部75cm范围内,占88％.据此建议土壤施药化学防治沟眶象时,施药深度不宜低于45cm,施药点距树干基部水平距离不得少于75cm,且树周各个方向均需施药.每年10月末沟眶象开始“人土”、翌年4月末开始“出土”,在沟眶象“人士”结束后但未冻土之前的11中旬和土壤解冻之后但尚未“出土”前的4月中旬,这两个时期土壤施药防治效果较好;防治沟眶象的同时,还应适时采取打孔注药、熏蒸等措施防治臭椿(Ailanthus altissima(Mill.)Swingle)树干内的臭椿沟眶象Eucryptorrhynchus brandti(Harold).     

宁夏灵武市沟眶象发生特点

系统调查沟眶象Eucryptorrhynchus chinensis(Olivier)在宁夏灵武市的发生情况和特点发现:沟眶象以成虫和幼虫在土壤中越冬,成虫有2个发生高峰期,越冬结束后以成虫越冬的沟眶象出土出现第1个高峰期,以幼虫越冬的沟眶象经化蛹羽化出土出现第2个高峰期;幼虫危害臭椿根部形成的瘤状物可以作为鉴别沟眶象危害的特征;沟眶象幼虫在土壤中垂直分布范围集中在0～45 cm深土层,约占80%;成虫出土孔集中在距臭椿树干基部75 cm范围内,占88%。据此建议土壤施药化学防治沟眶象时,施药深度不宜低于45 cm,施药点距树干基部水平距离不得少于75 cm,且树周各个方向均需施药。每年10月末沟眶象开始"入土"、翌年4月末开始"出土",在沟眶象"入土"结束后但未冻土之前的11中旬和土壤解冻之后但尚未"出土"前的4月中旬,这两个时期土壤施药防治效果较好;防治沟眶象的同时,还应适时采取打孔注药、熏蒸等措施防治臭椿(Ailanthus altissima(Mill.)Swingle)树干内的臭椿沟眶象Eucryptorrhynchus brandti(Harold)。     

三种杀虫剂对昆虫病原线虫侵染臭椿沟眶象幼虫能力的影响

昆虫病原线虫在20世纪初后已发展成为生物防治领域研究热点之一,作为生防制剂被广泛使用,且可与杀虫剂混用.臭椿沟眶象Eucryptorrhynchus brandti是重要的林木蛀干害虫,对宁夏农田防护林主要树种臭椿Ailanthus altissima造成严重危害.目前臭椿沟眶象的主要防治方法之一是化学防治,但效果不理想.为了降低对臭椿沟眶象幼虫的农药使用剂量并提高防治效果,须筛选与昆虫病原线虫混用适合的杀虫剂.本研究测试了4.5％氯氰菊酯乳油、10％吡虫啉可溶液剂、5％啶虫脒乳油对小卷蛾斯氏线虫Steinernema carpocapsae All、长尾斯氏线虫Steinernema longicaudum X-7存活以及侵染率的影响,以筛选对臭椿沟眶象3龄幼虫致死效果好、能与昆虫病原线虫混用的杀虫剂和混用配比.结果 表明,3种杀虫剂对2种线虫的存活均无亚致死作用;吡虫啉对2种线虫的致死率无明显影响;不同浓度的氯氰菊酯和啶虫脒对2种线虫的致死率存在显著差异,其中有效成分为88.97 μg/mL、17.79 μg/mL的氯氰菊酯和有效成分为307.89 μg/mL、61.58 μg/mL的啶虫脒对2种线虫的致死率均显著高于对照.3种药剂与X-7、All混用对臭椿沟眶象3龄幼虫均表现为增效或叠加作用,其中有效成分为8.89 μg/mL的氯氰菊酯和有效成分为7.67 μg/mL的吡虫啉与线虫X-7混用对臭椿沟眶象3龄幼虫表现出增效作用,致死率分别为41.67％、54.17％,其它浓度和其它药剂与2种线虫混用的各处理均表现为叠加作用.该结果为进一步利用昆虫病原线虫开展野外防治试验奠定了基础.     

基于沟眶象属两近缘种不同虫态转录组的气味受体基因鉴定及表达分析

【目的】基于沟眶象属Eucryptorrhynchus两近缘种沟眶象E. scrobiculatus和臭椿沟眶象E. brandti不同虫态的转录组数据进行气味受体(odorant receptor, OR)基因的鉴定及表达特征分析,补充两种象甲的气味受体信息,为之后的功能研究提供理论依据。【方法】从沟眶象(幼虫、蛹和成虫)和臭椿沟眶象(卵、幼虫、蛹和成虫)不同虫态转录组数据库中筛选OR基因序列;基于两种象甲触角转录组数据,对两种象甲筛选得到的ORs进行种间和种内的序列比对;利用最大似然法对两种象甲新鉴定的ORs进行系统发育分析;根据两种象甲不同虫态转录组数据中OR基因的FPKM(fragments per kilobase per million mapped fragments)值对新鉴定的OR基因进行表达丰度分析;利用qPCR检测新鉴定的OR基因在沟眶象和臭椿沟眶象不同发育阶段和成虫不同组织中的表达谱。【结果】从沟眶象和臭椿沟眶象不同虫态转录组数据库中分别鉴定出6和4个OR基因,都具有完整的开放阅读框。根据与触角转录组数据的序列比对结果,从沟眶象和臭椿沟眶象分别新鉴定出4个(EscrOR50-53)和2个(EbraOR46-47)OR基因;在两象甲种间发现了一对可能的同源基因EscrOR53和EbraOR45。系统发育树显示,6个新鉴定的OR蛋白分属于鞘翅目OR亚家族2B和7。结合不同虫态转录组的FPKM数据及qPCR检测的时空表达谱得知,沟眶象3个和臭椿沟眶象2个新鉴定到的OR基因均在成虫的非嗅觉组织中高表达,且在卵、幼虫或蛹期也有表达。【结论】本研究明确了沟眶象和臭椿沟眶象不同虫态转录组中的气味受体基因及其时空表达谱,并且发现两种象甲的生殖器官中可能存在非嗅觉的功能性的ORs,提示其可能在发育的早期阶段就已发挥功能。     

沟眶象和臭椿沟眶象对不同诱源的趋性比较

沟眶象Eucryptorrhynchus scrobiculatus和臭椿沟眶象Eucryptorrhynchus brandti是中国北方严重危害臭椿的钻蛀性害虫。为开发这两种象虫的诱捕技术,本文比较了8种不同波长的LED灯、黑光灯、频振式杀虫灯,糖醋液和臭椿木段对两种象甲的引诱效果,并在室内、野外进行回捕试验。室内不同诱源选择结果表明,沟眶象对臭椿木段最敏感,臭椿沟眶象对频振式杀虫灯最敏感;在室内,臭椿木段对沟眶象的回捕率最高,频振式杀虫灯对臭椿沟眶象的回捕率最高;在野外,频振式杀虫灯对沟眶象和臭椿沟眶象的回捕率均最高。本研究建议使用频振式杀虫灯监测和防治沟眶象和臭椿沟眶象。     

臭椿沟眶象成虫越冬场所选择的关键因子

昆虫成虫越冬前会选择合适的越冬场所,为了更好地控制臭椿沟眶象Eucryptorrhynchus brandti(Harold)成虫,需要了解其越冬场所的特点,找出影响其越冬场所选择的关键因素,以便开展越冬场所管理和翌年发生预测。在宁夏臭椿沟眶象发生区,采用平行线取样方法中的随机调查法调查臭椿沟眶象越冬场所(寄主、寄主树下植被、土壤温湿度)、越冬的树干方位、越冬位置距树干距离等情况。用皮尔逊相关性与多元统计分析方法确定影响其越冬的主要因素为胸径(X_1)、流胶孔数(X_2)、羽化孔数(X_2)、土壤湿度(X_3)、越冬土壤深度(X_5)、越冬树干方位(X_7)对臭椿沟眶象越冬成虫数量有显著影响(P≤0.05),建立的多元回归模型为Y=-26.267+0.258X_1-1.138X_2+5.276X_3+0.824X_5+20.191X_7-0.707X_(10),R~2=0.586,正判率为63.4%。对越冬成虫数量的实测值与预估值进行t-检验,发现预估值与实测值之间无显著差异(P=0.103≥0.05)。建立的多元回归模型,能够预测翌年害虫发生情况,利用其选择越冬场所的特点,为开展臭椿沟眶象潜所诱杀提供理论依据。     

臭椿沟眶象的发生和防治

<正> 近年来,臭椿沟眶象Eucryptorrhynchus brandti(Harold)在连云港地区发生较普遍。幼虫期蛀食臭椿Ailanthus altissima Swingle距地面2m以下的韧皮部或木质部,春季成虫为害臭椿幼树顶芽、侧芽或叶柄,造成芽萎蔫和     

光滑足距小蠹消化道的解剖结构

采用体视显微和扫描电镜技术研究光滑足距小蠹Xylosandrus germanus(Blandford)消化道的解剖结构。结果表明,光滑足距小蠹消化道由前肠、中肠和后肠三部分组成。成虫前胃由8个骨化的前胃板组成,呈灯笼状结构。前胃板由板状部和片状部组成,板状部短而简单,片状部甚长,由斜面、咀嚼刷和关闭刚毛组成。胃盲囊着生在中肠近后端,有细管状和囊状2种,成虫分别有1对,幼虫有1对细管状和3~5对囊状。6根马氏管分成2组,1组4根,另一组2根。6根马氏管与后肠肠壁形成隐肾系统。消化道具有1对囊状和1对细管状的胃盲囊可作为光滑足距小蠹成虫的识别特征。     

胸窗萤幼虫对灰巴蜗牛的捕食机制初探

本文对胸窗萤Pyrocoelia pectoralis Oliver 4龄幼虫捕食灰巴蜗牛Bradybaena ravida Benson的机制进行了初步探索。通过解剖幼虫消化道进行观察,发现幼虫的食道在与上颚基部骨化结构相连处分为2支,呈Y型结构,分别与2个上颚的中空管道相通;无毒腺结构存在。将幼虫头部及消化道各部分提取液注射到灰巴蜗牛体内后发现中肠提取液对蜗牛的致死效果显著高于头部和消化道其它部分提取液对蜗牛的致死效果(df=68,P<0.05),比较不同浓度中肠提取液对蜗牛致死效果的差异后发现,浓度为5 mg/mL的中肠提取液对蜗牛的致死时间(15.96±4.48)min与幼虫正常捕食的时间(14.47±2.32)min最为相近。     

斜纹夜蛾幼虫肠道不同部位对Zn2+积累作用的比较研究

在人工饲料中添加不同浓度的Zn2+连续胁迫3个世代的斜纹夜蛾Spodoptera litura Fabricius幼虫,采用等离子体原子发射光谱仪检测分析了连续3个世代6龄幼虫肠道不同部位对食物中Zn2+的积累作用.结果表明,Zn2+可在六龄幼虫前、中和后肠中积累,积累量受到食物中Zn2+的浓度和胁迫世代数的双重影响.每个世代6龄幼虫前肠、中肠和后肠中的Zn2+含量均随着饲料中Zn2+浓度增加而增加.六龄幼虫肠道3个不同部位对Zn2+的积累作用依次为前肠＜中肠＜后肠.而随着胁迫世代数的增加,不同世代6龄幼虫前肠、中肠和后肠中的Zn2+含量表现出显著减少的趋势.因此,植食性昆虫消化道不同部位对食物中Zn2+的积累作用有所不同,并随着胁迫世代数的增加而显著减少.     

蔡家河湿地土壤种子库特征及其与地上植被和土壤因子的关系

为明确蔡家河湿地土壤种子库特征及其与地上植被和土壤因子的关系, 采用野外调查取样和室内萌发实验相结合的方法, 对芦苇群落, 野艾蒿群落和林下杂草群落3种不同植被类型的土壤种子库密度, 物种组成, 地上植被以及土壤理化性质进行了调查研究。结果表明: 蔡家河湿地3种植被类型的土壤种子库密度分别为(7725±1286) 粒•m-2, (2535±556) 粒•m-2和(5085±984) 粒•m-2; 物种数量分别为36种, 28种和39种。3种植被类型土壤种子库的物种丰富度以及多样性均高于地上植被, 并且3种植被类型间土壤种子库物种组成的相似性高于地上植被, 说明土壤种子库比地上植被具有更高的稳定性。芦苇群落的种子库密度, 物种多样性指数以及土壤种子库和地上植被物种组成的相似性均高于野艾蒿群落和林下杂草群落。土壤含水量与土壤有机质是影响土壤种子库物种组成的主要土壤因子, 在土壤水分以及有机质含量高的芦苇群落中含有大量湿生植物种子, 但在水分和有机质含量低的野艾蒿和林下杂草群落未发现柳叶菜(Epilobium hirsutum)、马先蒿(Pedicularis resupinata)、问荆(Equisetum arvense)等湿生植物的种子。因此, 蔡家河湿地土壤种子库已出现一定程度的退化, 芦苇群落土壤种子库可用作退化湿地植被恢复的种源, 在植被恢复时要满足种子萌发对土壤水分和有机质的需求。     

新型2-喹诺酮类Polo样激酶1抑制剂的设计合成及分子对接研究

目的:设计合成新型2-喹诺酮类Polo样激酶1(Plk1)抑制剂。方法:以Plk1抑制剂ON 01910为先导化合物,利用生物电子等排原理设计一系列2-喹诺酮类衍生物,用Autodock软件将该类化合物与Plk1进行分子对接和虚拟筛选,计算结合自由能;以取代的氯(溴)苄为起始原料,先后经巯基乙酸取代、双氧水氧化、与(对甲氧基)苯胺酰化,再经环合、水解制得目标化合物。结果:设计的化合物大多数与Plk1的结合自由能均比ON 01910的低,结合强度高、稳定性好;合成了16个2-喹诺酮类衍生物,产物结构经1H-NMR确证。结论:所得化合物中有15个为新化合物,化合物的结构设计科学合理,虚拟筛选结果良好,为后续实体筛选和化合物结构优化提供了理论依据和参考。     

抗肿瘤药物Rigosertib研究进展

Rigosertib是一种非ATP竞争性多激酶抑制剂,具有显著的抗有丝分裂和抗癌活性,可诱导多种肿瘤细胞增殖停滞和凋亡,对正常细胞增殖的影响很小。Rigosertib已作为高危骨髓增生异常综合征患者的治疗药物应用于Ⅲ期临床试验。本文就Rigosertib的分子作用机制、体内外抗肿瘤活性以及临床试验等方面的研究进展做简要综述。     

封育年限对岩溶植被组成和土壤肥力修复的影响

岩溶植被修复是国家重大战略需求,为揭示封育年限对岩溶植被组成和土壤肥力修复的影响,该研究以空间代替时间的方法,选择不同封育年限的草丛(封育5 a)、灌丛(15 a)、灌乔林(25 a)、次顶极乔林(35 a)和顶极乔林(55 a)作为研究对象,调查分析不同封育年限岩溶植被组成和土壤肥力的特征及其修复机制。结果表明:研究样地(18 000 m ^2)共有维管植物175种,隶属74科139属,不同封育年限群落科属种组成明显不同,以封育5 a的最低(6科19属20种),封育35 a的最高(48科74属88种)。随着封育期延长,乔木生活型比例显著增加,灌木为先增后减,草本急剧减少,藤本先增后减。随着进展演替,群落不同层次的优势种替代规律不同,草本层为阳性杂草→阳性禾草→中生性或阴生性蕨类植物的有序性替代;灌木层为灌木种类被乔木幼苗幼树所替代;而乔木层却表现为常绿种类占优势到常绿与落叶树种共优势的结构性替代。封育初期群落物种组成简单,多样性较低,土壤有机质、全氮、有效氮含量较低,进入中期(25 a),多样性升高,土壤养分含量也增高,进入后期(55 a),多样性降低,土壤养分含量也相应下降,但维持在较高水平,表现出较强的协同修复效应。冗余分析(RDA)表明,群落物种组成在封育初期受土壤容重(SBD)、毛管孔隙度(CP)、全钾(TK)、速效钾(AK)、速效磷(AP)的显著影响,而在中后期则受土壤有机质(SOM)、水分含量(MC)、非毛管孔隙度(NCP)、全氮(TN)、有效氮(AN)以及碳氮磷化学计量比的显著影响。     

Processing character of the action of wheat endonucleases WEN1 and WEN2. Kinetic parameters

The wheat seedling endonucleases WEN1 and WEN2 dependent on Mg²⁺, Ca²⁺, and S-adenosyl-L-methionine (SAM) and sensitive to the substrate DNA methylation status have an expressed processing action. The enzymes hydrolyze DNA at a few subsequent stages: first, they split λ phage DNA specifically at CNG-sites (WEN1) with liberation of large fragments; second, they hydrolyze these fragments to 120–140 bp oligonucleotides that finally are hydrolyzed to very short fragments and mononucleotides. Initial stages of DNA hydrolysis may proceed in the absence of Mg²⁺, but subsequent hydrolysis stages are very strongly stimulated by Mg²⁺. It cannot be ruled out that modulation of enzymatic activity with Mg²⁺ and probably with DNA fragments formed is associated with reorganization of the structure of eukaryotic (wheat) endonucleases with respective changes in their catalytic properties and site specificity of action. Michaelis constant value for WEN1 endonuclease on hydrolysis of methylated λ phage DNA containing Cm⁵CWGG and Gm⁶ATC sites is four-fold lower compared with that observed on hydrolysis of unmethylated λ phage DNA. This may indicate that affinity of WEN1 enzyme to methylated DNA is higher than that to unmethylated DNA. In the presence of SAM, the Michaelis constant for WEN2 on the DNA hydrolysis stage characterized by formation of 120–140 bp fragments is decreased, but for WEN1 it is increased by 1.5–2.0-fold. This means that SAM inhibits WEN1 but stimulates WEN2. Thus, wheat endonucleases WEN1 and WEN2 differ significantly in affinities to substrate DNAs with different methylation status, in velocities of DNA hydrolysis, and time of production of DNA fragments of similar length. It seems that the investigated plant endonucleases can hydrolyze DNA in the nucleus as well to both large and very short fragments including mononucleotides, that is, in particular, essential for utilization of cell nucleic acid material during apoptosis.     

Modulation of action of wheat seedling endonucleases WEN1 and WEN2 by histones

Wheat core histones and various subfractions of histone H1 modulate differently the action of endonucleases WEN1 and WEN2 from wheat seedlings. The character of this modulation depends on the nature of the histone and the methylation status of the substrate DNA. The modulation of enzyme action occurs at different stages of processive DNA hydrolysis and is accompanied by changes in the site specificity of the enzyme action. It seems that endonuclease WEN1 prefers to bind with protein-free DNA stretches in histone H1-DNA complex. The endonuclease WEN1 does not compete with histone H1/6 for DNA binding sites, but it does compete with histone H1/1, probably for binding with methylated sites of DNA. Unlike histone H1, the core histone H2b binds with endonuclease WEN1 and significantly increases its action. This is associated with changes in the site specificity of the enzyme action that is manifested by a significant increase in the amount of low molecular weight oligonucleotides and mononucleotides produced as a result of hydrolysis of DNA fragments with 120–140-bp length. The WEN2 endonuclease binds with histone-DNA complexes only through histones. The action of WEN2 is increased or decreased depending on the nature of the histone. Histone H1/1 stimulated the exonuclease activity of WEN2. It is supposed that endonucleases WEN1 and WEN2, in addition to the catalytic domain, should have a regulatory domain that is involved in binding of histones. As histone H1 is mainly located in the linker chromatin areas, it is suggested that WEN2 should attack DNA just in the chromatin linker zones. As differentiated from WEN2, DNA hydrolysis with endonuclease WEN1 is increased in the presence of core histones and, in particular, of H2b. Endonuclease WEN1 initially attacks different DNA sites in chromatin than WEN2. Endonuclease WEN2 activity can be increased or diminished depending on presence of histone H1 subfractions. It seems that just different fractions of the histone H1 are responsible for regulation of the stepwise DNA degradation by endonuclease WEN2 during apoptosis. Modulation of the action of the endonucleases by histones can play a significant role in the epigenetic regulation of various genetic processes and functional activity of genes.     

The EmhABC efflux pump decreases the efficiency of phenanthrene biodegradation by Pseudomonas fluorescens strain LP6a

Pseudomonas fluorescens strain LP6a, designated here as strain WEN (wild-type PAH catabolism, efflux positive), utilizes the polycyclic aromatic hydrocarbon phenanthrene as a carbon source but also extrudes it into the extracellular medium using the efflux pump EmhABC. Because phenanthrene is considered a nontoxic carbon source for P. fluorescens WEP, its energy-dependent efflux seems counter-productive. We hypothesized that the efflux of phenanthrene would decrease the efficiency of its biodegradation. Indeed, an emhB disruptant strain, wild-type PAH catabolism, efflux negative (WEN), biodegraded 44% more phenanthrene than its parent strain WEP during a 6-day incubation. To determine whether efflux affected the degree of oxidation of phenanthrene, we quantified the conversion of ¹⁴C-phenanthrene to radiolabeled polar metabolites and ¹⁴CO₂. The emhB ^? WEN strain produced approximately twice as much ¹⁴CO₂ and radiolabeled water-soluble metabolites as the WEP strain. In contrast, the mineralization of ¹⁴C-glucose, which is not a known EmhB efflux substrate, was equivalent in both strains. An early open-ring metabolite of phenanthrene, trans-4-(1-hydroxynaphth-2-yl)-2-oxo-3-butenoic acid, also was found to be a substrate of the EmhABC pump and accumulated in the supernatant of WEP but not WEN cultures. The analogous open-ring metabolite of dibenzothiophene, a heterocyclic analog of phenanthrene, was extruded by EmhABC plus a putative alternative efflux pump, whereas the end product 3-hydroxy-2-formylbenzothiophene was not actively extruded from either WEP or WEN cells. These results indicate that the active efflux of phenanthrene and its early metabolite(s) decreases the efficiency of phenanthrene degradation by the WEP strain. This activity has implications for the bioremediation and biocatalytic transformation of polycyclic aromatic hydrocarbons and heterocycles.     

人工湿地-微生物燃料电池耦合系统的研究进展

人工湿地-微生物燃料电池耦合系统(CW-MFC)是一种将人工湿地技术(CW)和微生物燃料电池技术(MFC)结合在一起的新型污水处理系统,其产电机理是产电微生物在底层湿地(阳极)的厌氧条件下生成电子,通过外电路传递到表面湿地(阴极)完成氧化还原反应。但是,近几年来,关于CW-MFC研究的文章较少且研究深度较浅。综述了电极材料、水力条件、湿地植物及微生物等条件对CW-MFC污水处理能力和产电能力的影响。在电极材料方面,选用导电性、吸附性及有效面积大的材料作为电极可有效提高CW-MFC产电与去污能力;在水利条件方面,在HRT为2-3 d的条件下,应选用升流式或升流-降流式的入水方式;湿地植物方面,种植湿地植物的CW-MFC在去污和产电能力上都要优于未种植植物的CW-MFC;微生物方面,阴极与阳极的微生物群落结构存在明显的差异,但存在的产电菌的种类却十分相似。CW-MFC中存在的常见产电微生物主要包括地杆菌属(Geobacter)、脱硫叶菌属(Desulfobulbus)、假单胞菌属(Pseudomona)和脱硫弧菌属(Desulfovibrio)等。最后对CW-MFC的研究方向进行了分析,以期为CW-MFC的实际应用提供理论依据。