树冠结构参数及附近风场特征的风洞模拟研究

根据风洞模型实验,分析了树冠结构参数（疏透度β、透风系数α）和际近的风速场特征,结果表明,透风系数与疏透度之间符合幂函数关系α＝β＾０．６,树冠附近的风速减弱区为椭球形立体空间,减弱区随树高,冠幅的增大而增大,随透风系数（或疏透度）的增大而减小,在水平和垂直剖面上,等风速线分别为椭圆形和椭圆线段。     

棉铃虫成虫对性信息素的电生理和行为反应研究

通过EAG和风洞实验,研究了棉铃虫雌雄成虫对性信息素组分和诱芯(Z-11-16Ald∶Z-9-16Ald=97∶3)的电生理反应。其中棉铃虫雌、雄蛾对诱芯的平均EAG反应测定值分别为1.06mV和4.32mV,分别高出对照(无性信息素空白诱芯)0.67mV和0.366mV,差异均达到极显著水平(雌蛾：t＝25.020, P≤0.01;雄蛾：t＝44.269,P≤0.01);棉铃虫雌蛾对性信息素组分(Z-11-16-Ald和Z-9.16Ald)的EAG反应值随浓度增加而增加;雄蛾在被剪除触角后与雌蛾不能正常交配,而雌蛾在被剪除触角后仍有40%的交配率,比正常雌雄蛾的交配率(70%)有所下降;在风洞实验中,雄蛾没有顺风远离诱源的飞行行为,趋向诱源的比率为81.8%,与对照有显著差异。研究表明性信息素组分对棉铃虫的交配活动有明显的影响。     

低覆盖度下两种行带式固沙林内风速流场和防风效果

研究在风速为10m/s和15m/s的风洞实验条件下,覆盖度为20%和25%的单行一带和两行一带模式乔木固沙林内的水平和垂直空间的风速变化情况,达到对两种不同模式的风速流场和防风效果进行比较分析的目的。通过分析得出:两种配置模式都形成了风影区和风速加速区相互组合的复杂的水平流场结构。两种模式对垂直空间风速影响相近,根据对不同高度风速的不同影响划分为微变化层(20-35 cm)、显著变化层(6-12 cm)和稳定变化层(0.4-3 cm)层次,两种模式在这几个层次风速表现出相同的变化规律。两行一带模式在第一带前降低水平空间风速的效果低于单行一带模式,第一带后高于后者。降低垂直空间风速规律为:对0.4-50 cm高度的风速均有一定的降低作用,0.4-12 cm高度的风速的降低效果较显著,且两行一带模式降低近地表(0.4 cm)风速的效果要高于单行一带模式。     

尺神经原位松解术与尺神经皮下前置术治疗肘管综合征近期疗效比较的回顾性研究

目的:比较尺神经原位松解术与尺神经皮下前置术治疗肘管综合征(CuTS)近期疗效。方法:本研究为回顾性研究,选取2016年7月～2017年7月期间我院二部收治的60例CuTS患者,根据手术方式的不同分为A组(n=32,尺神经原位松解术)和B组(n=28,尺神经皮下前置术),比较两组患者优良率、并发症、围术期指标、感觉运动功能(肌力、小指指端两点辨别觉、神经传导速度)以及DASH上肢功能障碍(DASH)评分。结果:B组术后12个月的优良率为92.86%(26/28),高于A组的68.75%(22/32)(P0.05)。两组术后并发症总发生率比较差异无统计学意义(P0.05)。两组术后12个月肌力、神经传导速度升高,且B组高于A组(P0.05),两组术后12个月小指指端两点辨别觉降低,且B组低于A组(P0.05)。两组术后3个月、术后6个月、术后12个月DASH评分呈下降趋势,且B组低于A组(P0.05)。B组手术切口长度、手术时间长于A组(P0.05),两组术后住院时间比较差异无统计学意义(P0.05)。结论:与尺神经原位松解术相比,尺神经皮下前置术治疗CuTS患者,虽然手术切口长度、手术时间相对较长,但其优良率更高,同时可有效恢复患者感觉运动功能及减轻其上肢功能障碍,且不增加并发症发生率,具有一定的临床应用价值。     

Hickory shuckworm Cydia caryana: electroantennogram and flight tunnel studies of potential sex pheromone components

Electroantennogram (EAG) measurement of male Cydia caryana moth antennal olfactory response to monounsaturated 12 and 14 carbon alcohols and acetates indicated that the (E)-8-, (E)-10- conjugated double bond system of a dodecadien-1-ol acetate is a critical chemical structural component of the C. caryana sex pheromone. Additionally, EAG measurements implicated (E)-8-dodecen-1-ol acetate, (Z)-8-dodecen-1-ol acetate, (Z)-9-dodecen-1-ol acetate and (Z)-12-tetradecen-1-ol as potential minor pheromonal components. An EAG dosage-response study suggested that there were at least two heterologous populations of pheromone acceptors. Behavioral analysis of male moth response in a flight tunnel to compounds which evoked the stronger EAG responses suggested that (E,E)-8,10-dodecadien-1-ol acetate and (Z)-9-dodecen-1-ol acetate resemble or are C. caryana sex pheromonal components, while (Z)-8-dodecen-1-ol acetate and (E)-10-dodecen-1-ol acetate are either parapheromones or are minor pheromone components. Behavioral significance of (Z)-12-tetradecen-1-ol was difficult to interpret in the flight tunnel.

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Résumé Les réponses olfactives antennaires de Cydia caryana, mesurées par électroantennogrammes (EAG), aux alcools et acétates à carbones monounsaturés en positions 12 et 14, ont montré que le système conjugué de double liaison, (E)-8-, (E)-10- du dodecadien-1-ol acétate constitue un composé chimique strutural critique de la phéromone sexuelle de C. caryana.De plus, les acétates: (E)-8-dodecen-1-ol,(Z)-8-dodecen-1-ol,(Z)-9-dodecen-1-ol, et le (Z)-12-tetradecen-1-ol, se sont révélés en AEG comme des composés secondaires de la phéromone. L'étude par AEG de la relation dose-réponse a conduit à l'hypothèse de deux catégories de populations de récepteurs de phéromones. L'analyse comportementale des résponses des papillons mâles dans le tunnel de vol aux composés qui ont provoqués les plus forts AEG, on fait estimer que les acétates (E,E)-8,10-dodécadien-1-ol et (Z)-9-dodecen-1-ol ressemblent (ou sont) les constituants de la phéromone sexuelle de C. caryana; tandis que les (Z)-8-dodecen-1-ol et (E)-10-dodecen-1-ol sont, soit des paraphéromones, soit des constituants mineurs de la phéromone.La signification biologique du (Z)-12-tétradécen-1-ol a été difficile à interprêter avec les expériences en tunnel de vol.

     

Sex pheromone components of female Cornutiplusia circumflexa

Capillary gas chromatography indicated the presence of (Z)-7-dodecenyl alcohol and (Z)-7-dodecenyl acetate in the abdominal tip extracts of female Cornutiplusia circumflexa (L.) (Lepidoptera: Noctuidae: Plusiinae) moths. Gas chromatography combined with mass spectrometry and dimethyl disulfide derivatization confirmed the structure of these two principal pheromone components. In a flight-tunnel bioassay, a 5:1 blend of alcohol and acetate elicited the complete courtship sequence by males. The response was comparable to that evoked by a live virgin female, but males spent significantly longer time at calling females than at the synthetic source. The 5:1 blend was also attractive to male C. circumflexa in the field, as indicated by catches in traps baited with this mixture. (Z)-7-dodecenyl alcohol alone was slightly attractive whereas (Z)-7-dodecenyl acetate alone was completely inactive. C. circumflexa is the first reported Plusiinae species which utilizes (Z)-7-dodecenyl alcohol as the major pheromone component.     

Effect of landscape heterogeneity on termite tunnel pattern: Simulation study

Although the environment in which termites live is very heterogeneous, most experimental studies on the termite tunnel patterns have been conducted on homogeneous sand substrates. In order to explore how the heterogeneity affects tunnel patterns, I developed an agent-based model to simulate termite tunneling behavior at the individual level. In this model, grid space consists of easy and difficult areas for tunneling. Heterogeneity, H, was defined as the degree of the mixture of the two areas. The tunnel patterns formed by changing the number of termites, N, and H were quantitatively characterized by territory circularity and the territory area. These patterns were categorized into two groups, one with a small territory area and high circularity (group 1) and the other with a large area and low circularity (group 2). Considering the previous study that the termite populations with high N values have high territorial scalability, it can be said that the territories belonging to group 2 have higher foraging abilities and viability than those belonging to group 1. The simulation results showed that the tunnel patterns generated for small N and high H belonged to group 2. This implies that the heterogeneity can make a positive contribution to the expansion of the foraging area by effectively focusing the foraging energy of a termite population. I briefly discussed the mechanism of this positive role and the limitations of this simulation study. In addition, I discussed issues that need to be resolved in the near future to overcome the limitations.     

Electrophysiological and behavioural evidence for a fourth sex pheromone component in the turnip moth, Agrotis segetum

Abstract. In addition to the pheromone components (Z)-5-decenyl, (Z)-7-dodecenyl and (Z)-9-tetradecenyl acetate (Z5-10:OAc, Z7-12:OAc and Z9-14:OAc), it has previously been shown that the sex pheromone gland of the turnip moth, Agrotis segetum (Lepidoptera: Noctuidae Schiff) contains 10:OAc, 12:OAc, Z5-12:OAc, Z9-12:OAc, 11–12:OAc, Z5-14:OAc, Z7-14:OAc and Z11-16:OAc. To find out whether any of these additional compounds is involved in the sex pheromone communication in A. segetum, a comprehensive electro-physiological and behavioural investigation was conducted. Single-sensillum recordings on male antennae revealed three subtypes of sensilla among the previously so-called Z5-10:OAc sensilla. One subtype was identified having one receptor neurone (A) that responded to Z5-10:OAc with a large spike amplitude and another neurone (B) that responded to (Z)-5-decenol (Z5-10:OH) with a small spike amplitude. In another subtype the B neurone responded to Z5-12:OAc and sometimes also to 27-12:OAc and 10:OAc, in addition to responding to Z5-10:OH. In a third subtype the A neurone responded to all acetates identified from the female pheromone gland, whereas the small spike amplitude neurone was tuned to Z5-10:OH. A flight tunnel assay showed that blends composed of nine, eight or seven compounds were equivalent to the previously identified three-component pheromone blend in eliciting male behavioural responses. In field trapping tests, blends of eleven, nine or seven compounds did, however, catch significantly more moths than the three-component blend. Further assays showed that only 25- 12:OAc could significantly increase the catch numbers when added to the three-component blend, and thus qualified as a fourth pheromone component in A. segerum. The behavioural significance of additional female-produced acetates — for which males possess antennal receptors — is suggested, but may be impossible to confirm because of ‘diminishing returns’ when trying to refine a multicomponent pheromone further.     

Flight of the honey bee VI: energetics of wind tunnel exhaustion flights at defined fuel content,speed adaptation and aerodynamics

To gain information on extended flight energetics, quasi-natural flight conditions imitating steady horizontal flight were set by combining the tetheredflight wind-tunnel method with the exhaustion-flight method. The bees were suspended from a two-component aerodynamic balance at different, near optimum body angle of attack and were allowed to choose their own speed: their body mass and body weight was determined before and after a flight; their speed, lift, wingbeat frequency and total flight time were measured throughout a flight. These values were used to determine thrust, resultant aerodynamic force (magnitude and tilting angle), Reynolds number, total flight distance and total flight impulse. Flights in which lift was body weight were mostly obtained. Bees, flown to complete exhausion, were refed with 5, 10, 15 or 20 l of a 1.28-mol·l^-1 glucose solution (energy content w=18.5, 37.0, 55.5 or 74.0 J) and again flown to complete exhaustion at an ambient temperature of 25±1.5°C by a flight of known duration such that the calculation of absolute and relative metabolic power was possible. Mean body mass after exhaustion was 76.49±3.52 mg. During long term flights of 7.47–31.30 min similar changes in flight velocity, lift, thrust, aerodynamic force, wingbeat frequency and tilting angle took place, independent of the volume of feeding solution. After increasing rapidly within 15 s a more or less steady phase of 60–80% of total flight time, showing only a slight decrease, was followed by a steeper, more irregular decrease, finally reaching 0 within 20–30 s. In steady phases lift was nearly equal to resultant aerodynamic force; tilting angle was 79.8±4.0°, thrust to lift radio did not vary, thrust was 18.0±7.4% of lift, lift was somewhat higher/equal/lower than body mass in 61.3%, 16.1%, 22.6% of all totally analysable flights (n=31). The following parameters were varied as functions of volume of feeding solution (5–20 l in steps of 5 l) and energy content. (18.5–74.0 J in steps of 18.5 J): total flight time, velocity, total flight distance, mean lift, thrust, mean resultant aerodynamic force, tilting angle, total flight impulse, wingbeat frequency, metabolic power and metabolic power related to body mass, the latter related to empty, full and mean (=100 mg) body mass. The following positive correlations were found: L=1.069·10^-9 f ^2.538; R=1.629·10^-9 f ^2.464; P _m=7.079·10^-8 f ^2.456; P _m=0.008v+0.008; P _m=18.996L+0.022; P _m=19.782R+0.021; P _m=82.143T+0.028; P _m=1.245·bm _f ^1.424 ; P _{mrel e}=6.471·bm _f ^1.040 ; =83.248+0.385. The following negative correlations were found: V=3.939–0.032; T=1.324·10^-4–0.038·10^-4. Statistically significant correlations were not found in T(f), L(), R(), f(), P _m(bm _e), P _{m rel e}(bm _e), P _{m rel f}(bm _e), P _{m rel f}(bm _f).Abbreviations A(m²) frontal area - bl(m) body length - bm(mg) body mass - c(mol·1^-1) glucose concentration of feeding solution - c _D (dimensionless) drag coefficient, related to A - D(N) drag - F _w(N) body weight - F _wp weight of paper fragment lost at flight start - f wingbeat frequency (s^-1) - g(=9.81 m·s^-2) gravitational acceleration - I(Ns)=R(t) dt total impulse of a flight - L(N) lift vertical sustaining force component - P _m(J·s^-1=W) metabolic power - P_{m ret} (W·g^-1) metabolic power, related to body mass - R(N) resultant aerodynamic force - Re v·bl·v ^-1 (dimensionless) Reynolds number, related to body length - s(m) v(t) dt virtual flight distance of a flight - s(km) total virtual flight distance - T (N) thrust horizontal force component of horizontal flight - T _a (°C) ambient temperature - t(s) time - t _tot (s or min) total flight time - v(m·s^-1) flight velocity - v(l) volume of feeding solution - W (J) energy and energy content of V - ( °) body angle of attack between body longitudinal axis and flow direction - ( °) tilting angle ( 90°) between R and the horizont in horizontal flight v(=1.53·10^-5m²·s^-1 for air at 25°) kinematic viscosity - (=1.2 kg·m^-3 at 25°C) air density