不同温度、土壤含水量及日光照时数对棉露尾甲虫(Haptoncus luteolus (Erichson))生长发育的影响

在5,10,15,20,30 ℃等5种温度、10%,20%,30%等3种土壤含水量和8,12,16 h等3种日光照时数共45个处理组合条件下,以丝瓜花作为饲料研究了3个因素对棉露尾甲生长发育的联合作用。结果表明：适合于卵生长发育的处理组合为25~35 ℃、10~15%和12~16 h,其中最佳处理组合为30 ℃、10%和12 h,在此组合条件下,卵发育历期为0.8 d,孵化率为93.3%;适合于幼虫及蛹生长发育的处理组合为：25~30 ℃、10~15%和12~16 h,其中最佳处理组合分别为30 ℃、10%、12 h和30 ℃、10%、8 h,在此组合条件下,幼虫历期、存活率和蛹历期、羽化率分别为5.0 d、85.7%和2.2 d、83.3%。在三元二次回归模型中,卵、幼虫、蛹和整个未成熟期（卵至蛹的历期）发育进度最快时的处理组合分别为27.5 ℃、10%、8 h,30 ℃、20%、12 h,32.5 ℃、10%、16 h和30 ℃、10%、16 h;此时理论最短历期分别为0.8、4.4、1.4 d和7.3 d。     

温度对传粉甲虫——棉露尾甲生长发育、存活及繁殖的影响

在光照周期为 12 L:12 D、土壤含水量为 15 %的 5种恒温条件下 (15℃、2 0℃、2 5℃、30℃和 35℃ ) ,以丝瓜花为饲料研究了棉露尾甲未成熟期 (卵期、幼虫期和蛹期 )的生长发育和存活情况 ;同时 ,在同样的光照和温度、棉球保湿的条件下 ,研究了温度对成虫寿命及繁殖的影响情况。结果表明 ,未成熟期各虫态发育速率随温度呈抛物线变化 ,30℃时发育速率最大 ;15℃时卵孵化率最高 ,2 0～ 30℃时 ,幼虫存活率、蛹羽化率显著高于低温 (15℃ )和高温 (30℃ ) ,平均分别可达 96 .3%和 93.2 % ,低温和高温对其有明显的抑制作用 ;成虫寿命同温度之间呈负的线性关系 ,雌虫寿命普遍长于雄虫 ,30℃时雌虫的产卵期最长 ,繁殖力最大 ,最高可达 14 6粒 /雌 ,产卵期和产卵量与温度之间呈抛物线关系     

食料含水量对黄斑露尾甲生长发育和生殖的影响

黄斑露尾甲适宜高湿的生境。室内试验结果表明,食料含水量15％时,卵完全不能孵化。在食料含水量20～45％范围内,卵孵化率、幼虫发育速率及成虫日均产卵量均与食料含水量之间呈“S”形曲线关系,拟合关系式分别为和;幼虫期死亡率与食料含水量之间呈二次曲线关系,拟合关系式为D=0.2926W~2-20.8121W+379.3,并求得幼虫期死亡率最低的食料含水量为35.6％;预蛹和蛹则不甚敏感,其发育速率和死亡率均随食料含水量变化而定。     

棉露尾甲发育起点温度和有效积温的研究

在 1 5 ,2 0 ,2 5 ,3 0和 3 5℃下 ,测定了棉露尾甲Haptoncusluteolus(Erichson)各虫态的发育历期。结果表明 ,卵到蛹各虫态历期随温度升高而呈抛物线变化 ,3 0℃时发育历期最短 ;成虫寿命及世代历期随温度升高呈负线性变化。对试验结果采用了 2种方法计算发育起点温度和有效积温 ,并用变异系数进行检验。结果表明 ,除预蛹期外 ,其它各虫态用最优化法计算结果优于直线回归法 ,卵、幼虫、预蛹、蛹、雌雄成虫产卵前期的发育起点温度分别为 :9 9,7 9,8 6,9 5 ,1 3 0 ,1 3 3和 5 7℃ ,有效积温分别为 :2 6 4,5 3 9,5 4 91 5 1 6,1 3 4 1 ,5 2 4和 3 2 2 0日·度 ;预蛹期的发育起点温度和有效积温分别为 4 8℃和 94 1日·度。     

棉露尾甲在不同饲料上的生长发育及繁殖力比较

【目的】棉露尾甲Haptoncus luteolus Erichson是棉花和番荔枝科等植物上重要的传粉昆虫,研究其室内人工饲养技术对于开发其传粉价值和以其为对象进行转基因棉花安全性评价等方面具有重要意义。【方法】利用筛选的人工饲料和油菜花粉2种潜在的人工饲料,同时以天然饲料丝瓜花为对照,观察比较棉露尾甲初孵幼虫在3种饲料上的生长发育及羽化为成虫后的繁殖力差异。【结果】棉露尾甲初孵幼虫在3种饲料上发育至成虫的生存曲线无显著差异;与丝瓜花和油菜花粉相比,人工饲料饲养棉露尾甲的幼虫期缩短,蛹期延长;人工饲料饲养的雌成虫羽化后20d内累计产卵量显著高于丝瓜花和油菜花粉处理,且可以维持较长时间的单日高产卵量,从而显著提高繁殖力。【结论】人工饲料饲养的棉露尾甲生物学特征与丝瓜花饲养的相似,但繁殖力显著提高,可以利用人工饲料结合配套的饲养技术进行棉露尾甲的室内长期大量饲养。     

不同温度和土壤含水量对大斑芫菁生长发育的联合作用

在室内人工饲养大斑芜蓄,研究了不同温度、土壤台水量对大斑芜蓄生长发育及其卵的孵化串的联合作用。结果表明：大斑芜蓄不同生长发育时期对温度、土壤台水量的要求有所不同,１—６龄幼虫发育速率最快时的温度和土壤台水量依次为：３２．６℃、６％;３５．６℃、６％;３６．３℃、６％;３８．０℃、６％;３５．６℃、６％;３８．０℃、７．１％,蛹发育速率最快时的温度、土壤台水量为３７．１℃、６％。卵孵化率最高时的温度、土壤台水量为３４．０℃、１２％,卵发育速率最快时的温度、土壤台水量为３３．２℃、７％,     

温度和土壤含水量对青冈栎种子萌发的影响

运用直播法,研究应用人工气候箱控制温度和土壤含水量对野生青冈栎种子萌发和幼苗生长的影响。结果表明:在12h光照条件下,青冈栎种子在变温为10℃/15℃时,萌发率很低,仅为(12±12.29)%;变温为30℃/35℃时,萌发率达最大,为(81±13.7)%。土壤含水量为30%～40%时,萌发率为(79±15.9)%;土壤含水量为90%～100%时,萌发率为(56.67±19.36)%。青冈栎种子萌发呈现出迅速萌发和推迟萌发的特点;温度对青冈栎幼苗的苗高、叶长和叶宽影响显著,对幼苗的地径、叶片数量影响不显著。恒温下,不同梯度土壤含水量处理对幼苗的苗高、地径、叶长、宽影响不显著。     

温度及土壤含水量对淡剑纹灰翅夜蛾死亡率的影响

淡剑纹灰翅夜蛾Spodopteradepravata(Bulter)在 2 2 ,2 5 ,2 8,3 1 ,3 4,3 6,3 8℃恒温条件下卵孵化率分别为 96. 0 0 ,91 .0 0 ,83. 90 ,84. 81 ,83 . 60 ,80 %和 0。高龄幼虫在低温环境下 ,一般随温度的降低、时间的延长死亡率增加。过冷却点为 (-6. 81± 1 . 63 )℃ ,体液冰点为 (-3 .5 1± 1 . 5 6)℃。 1 0 %土壤含水量时该虫羽化率最高 ,40 %及其以上羽化率为 0。     

不同温度对烟草生长发育及光合作用的影响

该试验通过人工气候室模拟相对低温(日均温16.5℃)、常温(日均温23.5℃)和相对高温(日均温30.5℃)3种日动态温度,研究了不同温度对烟草生长发育及光合作用的影响。结果表明:(1)与常温下生长的烟草相比,相对低温和高温处理均降低了烟株的株高、叶长和叶宽,在一定程度上抑制了烟草的生长。(2)相对低温和高温处理比常温处理下有较低的烟叶净光合速率(Pn)、胞间CO_2浓度(Ci)、气孔导度(Gs)、蒸腾速率(Tr)、PSⅡ最大光化学量子效率(F_v/F_m)、PSⅡ实际光化学量子效率(ΦPSⅡ)、光化学猝灭系数(qp)、Rubisco羧化酶活性和相对较高的初始荧光强度(F0)。长期较高或较低的温度均会对烟草的生长发育产生抑制,这可能因其在一定程度上抑制了烟叶的光合机构活性并对反应中心造成了损伤,从而降低了烟草的光合作用,抑制了烟株的生长,长期日均温23.5℃有利于烟草的生长和光合作用。     

温度对棉大卷叶螟生长发育和繁殖的影响

本文利用生命表方法评价了温度对棉大卷叶螟生长发育和繁殖的影响.结果表明：在17 ℃～26 ℃温度范围内,棉大卷叶螟的发育历期随温度升高而显著缩短;当温度超过32 ℃时,其发育历期延长.棉大卷叶螟的世代起点发育温度为12.08 ℃,有效积温为436.2日·度.在17 ℃～35 ℃温度范围内,棉大卷叶螟的存活率在26 ℃下最高,其他温度下的存活率随温度的升高或降低而降低.在17 ℃～35 ℃之间,棉大卷叶螟实验种群的内禀增长率、世代净增殖率、周限增长率分别在29、26和32 ℃下最大,其值分别为0.1268、415.65和1.185.世代平均历期随着温度的升高而缩短,在17 ℃下最长,为89.11 d;在35 ℃下最短,为28.68 d.     

湿度和光照对桑白盾蚧种群生长的影响

本文分析了 4组不同湿度和 3组光照条件下桑白盾蚧 Pseudaulacapis pentagona(Targioni-Tozzetti)的种群生长状况 ,组建生命表。相对湿度在 55% ,77% ,80 % ,95%时 ,种群的内禀增长率分别为 :- 0 .0 0 57,0 .0 510 ,0 .0 50 8,0 .0 0 94 ;净增殖率分别为 :0 .6 92 0 ,2 7.2 10 0 ,2 7.6 6 80 ,1.86 0 6 ;后 3者世代增倍时间分别为 13.5910 ,13.6 4 4 6 ,73.7391天 ;光周期在 L∶D=14∶ 10 ,12∶ 12时 ,种群内禀增长率分别为 :0 .0 4 4 5,0 .0 334,净增殖率分别为 2 3.96 2 8,12 .156 2 ,增倍时间为 15.576 3,2 0 .752 0天 ,而 L∶D=10∶ 14时 ,净增殖率为 0 ,内禀增长率和增倍时间都不存在 ,种群将消亡。     

温度和光周期对斑翅食蚧蚜小蜂发育与繁殖的影响

斑翅食蚧蚜小蜂是橡副珠蜡蚧的重要寄生性天敌之一。研究了温度和光周期对斑翅食蚧蚜小蜂发育、寄生及繁殖等方面的生态学特性。研究表明:温度和光周期对斑翅食蚧蚜小蜂种群增长影响明显。在32℃下不能完成世代发育,在温度为18-27℃范围内随温度升高发育加快,18℃发育历期最长(54.0d),27℃最短(22.8d);世代发育起点温度和有效积温分别为12.76℃和307.62日度。高温和低温均不利于斑翅食蚧蚜小蜂寄生,21℃时寄生率最高为(36.0%),30℃时寄生率最低(4.5%)。结合发育历期、体长、产卵、抱卵、寄生率等参数,该蜂发育繁殖的适宜温度为21-27℃度范围内,30℃以上不利于小蜂的发育及存活。斑翅食蚧蚜小蜂对长光的刺激比较敏感,随光照时间增长,发育加快、产卵量明显增加,长日照条件(LD16∶8h)的发育历期最短(24.8d),短日照条件(LD10∶14h)的最长(27.8d),产卵量在长日照条件(LD16∶8h)时最多(119.6粒),短日照条件(LD10∶14h)时最少(86.2粒)。结合发育、产卵、寄生等参数,长日照条件(LD14∶10-LD16∶8h)有利于种群增长。     

海南山蛭对土壤湿度和气温的适应

在室内以土壤湿度梯度作为海南山蛭Haemadipsa hainana的栖息试验表明,海南山蛭栖息于含水量的15.1％－16.77％水分的土壤表面;野外调查表明,海南岛橡胶林内海南山蛭栖息于16.54％－17.66％含水量的土壤表面;热带雨林者栖息于19.92%-25.73%含水量的土壤,室内实验表明,海南山蛭爬向30－35℃温度范围,占试验蛭数79.15％,在8－9℃不活动,10℃能山蛭活动,随温度升高活动蛭数增加,而15℃试验蛭答部活动,活动蛭数与温度关系为Y－18.6Z-172.3,R-0.976,P=0.01。在橡胶林内8－9℃山蛭不活动;10℃开始有山蛭活动,且随温度升高活动蛭数增加,当17℃时所有山蛭活动,活动蛭数与温度关系Y＝4.73X-3.97,R=0.93,P=0.1。首次使用土壤湿度梯度测定山蛭对土壤湿度的要求,这是一个新的有普遍意义的方法,并讨论了海南山蛭对土壤湿度气温的适应。     

Effects of photoperiod and temperature on the development and diapause of the bark beetle Ips typographus

Abstract:  Diapause was induced in a Central European population of Ips typographus grown at 20°C when the day length decreased below 16 h [50% diapause incidence occurred in the 14.7:9.3 h L:D (light:dark) regime]. The non-diapausing adults fed on days 2–6 and 10–14 after the ecdysis and swarmed after the second feeding bout with chorionated eggs in the ovaries and sperm in the spermiducts. Neither gonads nor the flight muscles matured and no swarming occurred in the diapausing adults. The development from egg to adult took about 34 days in both 18:6 h (no diapause) and 12:12 h L:D (diapause) regimes, but it was extended by up to 30% without diapause induction when only larvae or pupae were exposed to L:D 12:12 h. Diapause was induced in insects reared at L:D 12:12 h through the last larval and the pupal instars and/or in the adult stage. Temperature ≥ 23°C prevented diapause induction at L:D 12:12 h but diapause occurred at L:D 14:10 h associated with 26:6°C thermoperiod. The effect of thermoperiods on the developmental rate requires further research. Exposure of the non-diapausing adults to 5°C for several days blocked feeding and evoked a diapause-like state, whereas diapausing adults fed and their gonads slowly developed at this temperature. Diapausing adults exposed in forest to low night temperatures and transferred in October to 20°C readily reproduced at 18:6, but not 12:12 h L:D photoperiods. After 2-months at 5°C and darkness, they became insensitive to the photoperiod, matured and most of them also swarmed at 20°C in the 12:12 h L:D regime. In a Scandinavian population, diapause occurred at 18:6 h L:D and was terminated either by exposure to 5°C or by very long photoperiod (L:D 20:4 h) combined with high temperature (23°C).     

Effects of temperature,photoperiod and soil humidity on induction of pseudopupal diapause in the bean blister beetle Epicauta gorhami

Larvae of the bean blister beetle Epicauta gorhami Marseul (Coleoptera: Meloidae) feed on grasshopper eggs in soil and undergo hypermetamorphosis. This beetle undergoes larval diapause in the fifth instar as a pseudopupa, a form characteristic of hypermetamorphosis in meloid beetles. The effects of temperature, photoperiod and soil humidity on larval development of E. gorhami are examined in a population in Miyazaki, Japan, using egg pods of Locusta migratoria L. as food. At lower temperatures (20 and 22.5 °C), all larvae become pseudopupae, regardless of the photoperiod. By contrast, at higher temperatures (27.5 and 30 °C), almost all larvae pupate at the end of the fourth instar, again regardless of the photoperiod. A long‐day photoperiodic response occurs only at an intermediate temperature (25 °C): under an LD 12 : 12 h photocycle, all larvae enter diapause, although the diapause incidence tends to decrease as the day length becomes longer. Pseudopupae are immobile and remain in diapause for ≥120 days when they are kept under the same conditions, except that diapause terminates within a relatively short time at 30 °C. Although lower soil humidity retards post‐feeding development, soil humidity has no effect on the diapause incidence. On the basis of the short developmental period and diapause avoidance under summer conditions, it is suggested that this beetle partially produces two generations a year in southwestern Japan.     

The regulation of development during diapause in Ephestia elutella (Hübner) by temperature and photoperiod

Diapausing larvae of Ephestia elutella reared at 20°C in short photoperiods (LD 11:13), and then maintained 12 weeks or longer at 5–15°C before transfer to 20 or 25°C, pupated sooner than unchilled controls. At 25°C, all samples kept in long photoperiods (LD 15:9) survived better and pupated faster than similarly treated samples held in short photoperiods (LD 9:15). Samples kept at 20°C after chilling pupated much slower than those at 25°C, and, except after exposure at 5°C, pupated at similar rates at LD 11:13 or 15:9, although mortality was higher at the shorter photoperiod. After exposure at 5°C, larvae required increased day-length as well as increased temperature to hasten pupation whereas after exposure at 10°C most responded to increased temperature only.For samples maintained in slightly heated or unheated outbuildings, the summer emergence was poorly synchronized and males on average emerged ahead of females. Samples moved from the unheated outbuilding to 25°C and long days in the laboratory in early spring, however, pupated quickly and males and females emerged together. A late phase of diapause development thus exists requiring both high temperature and long photoperiods to ensure a prompt resumption of morphogenesis. Spring temperatures in the United Kingdom are seldom high enough to synchronize the completion of diapause.     

温、湿度对美洲斑潜蝇发育、存活及食量的影响

以花斑芸豆Phaseolus vulgaris为食料植物,在不同温、湿度组合下,观测了美洲斑潜蝇Liriomyza sativae的发育、存活及取食特征。结果表明,卵、幼虫和蛹期的发育速率与温度的关系均呈S型曲线。发育起点温度为：卵,8.9℃;幼虫, 10.1℃;蛹,9.6℃;整个未成熟期,9.5℃。有效积温为：卵,57.7日·度;幼虫,53.9日·度;蛹,151.9日·度;整个未成熟期,264.2日·度。湿度对发育速率的影响不明显。温度对存活的影响较大,当温度>34℃或<19℃时,各虫态的存活率都显著降低。湿度对存活率的影响主要发生在蛹期,当湿度低于50%时,蛹的羽化率显著降低。在高温、低湿的条件下,蛹不能羽化。在相对低温下的累计取食面积大于高温时的相应值,在25℃时达到1.6 cm²,而在28℃及以上温度时取食面积只有0.9 cm²左右。