中华虎凤蝶栖息地、生物学和保护现状

本文为1992～1996年期间中华虎凤蝶分布和生物学研究结果的总结。中华虎凤蝶现仅分布在我国中部秦岭山脉和长江中下游一带,栖息地多为次生林,可分为长江中下游低地类型和秦岭山脉高山类型。低地类型的寄主植物为杜衡,人为干扰严重;高山类型的寄主植物为细辛,人为干扰较轻。中华虎凤蝶幼期发生历期和存活受光照、温度、湿度等气候因素影响显著。其种群分布格局属典型的异质种群类型。栖息地丧失和退化及寄主植物的过度人为利用是其持续生存的主要致危因素。其种群现状满足IUCN红色名录等级新标准下列条款：VULNERABLE :A1a, c, d + 2c,应定为易危物种。文中还提出了相应的保护对策和进一步研究的内容。     

温度与光周期对麝凤蝶生长发育的影响

观察了麝凤蝶的卵、幼虫和蛹在不同温度和光周期条件下的发育历期。结果表明 :卵、幼虫和蛹的发育起点温度分别为 1 3 7,7 9和 8 0℃ ,有效积温分别为 43 8,3 98 0和 2 79 4日·度 ;越冬蛹的发育可以分为 5个阶段 ;大部分越冬蛹在上午 (88 2 % )羽化 ;长光照处理平均比短光照出处理提前羽化 2d。     

温度对丝带凤蝶生长发育的影响

温度对丝带凤蝶生长发育的研究。结果表明,丝带凤蝶在武汉地区1年发生6代。在15~35℃范围内,卵孵化率、幼虫和蛹存活率分别在25,25和20℃时最高,卵、幼虫和蛹发育历期随温度升高显著缩短;适宜发育温度范围为20~35℃。丝带凤蝶卵、幼虫和蛹的发育起点温度分别约为(8.7±2.5)℃、(11.9±6.0)℃和(6.9±1.8)℃,有效积温分别约为(82.5±5.1),(222.2±39.5)和(178.7±7.3)日.度。     

中华虎凤蝶的生物学特性观察

中华虎凤蝶是世界珍稀蝶类。分布在我国长江以南的湖北长阳,江苏南京,江西九江,浙江杭州、天目山、平阳等地。近年来,由于植物破坏和被捕杀,数量日趋减少。我国已将之列为Ⅱ级保护动物。我们对该蝶进行了三年人工饲养和观察,现将结果简报如下。 年生活史 中华虎凤蝶在国内各分布地一年发生一代。以蛹在地表的枯枝落叶层中越冬。成虫出现期因各地气温不同而有差异。浙南为2月下旬,杭州3月上中旬,南京3月中下旬,天目山4月下旬至5月初,庐山5月上旬。我们在浙江丽水饲养三年,其年生活史见图1。     

中华虎凤蝶湖南种群栖息地特性及其生态保护策略

自2009年首次在湖南乌云界国家级自然保护区发现中华虎凤蝶种群以来,在该保护区持续开展了10余年的野外调查监测。通过对中华虎凤蝶湖南种群6个分布点的野外观测数据分析,结果表明中华虎凤蝶湖南种群栖息环境中的植被以禾本科、菊科、蔷薇科、百合科及豆科植物为主,共计有46科96属128种;不同栖息生境中种群数量差异较大,高山灌草丛为中华虎凤蝶湖南种群的主要生境,而梯田生境、乔木林生境中,其种群数量均很低,展现出与低矮芒草丛的保温遮阴特性以及寄主植物的分布密切相关。寄主植物的复壮和围栏的建设对中华虎凤蝶湖南种群的栖息环境起到了明显的保护作用、对其种群数量的增效作用显著。为深入研究中华虎凤蝶湖南种群的生物学和生态学特性提供了基础数据,为中华虎凤蝶湖南种群的保育工作开展奠定了理论基础,也为当地保护区的保护措施优化提供了科学依据。     

乌苏里虎凤蝶临江亚种的生活习性

乌苏里虎凤蝶临江亚种ＬｕｅｈｄｏｒｆｉａｐｕｚｉｌｏｉｌｉｎｊｉａｎｇｅｎｓｉｓＬｅｅ属古北区的蝶类 ,在中国、俄罗斯、朝鲜有种群分布[1～ 3] ,是东北地区风蝶科中体形最小、出现最早、蛹期最长的一种蝶类 ,具有较高的科研价值和观赏价值。其寄主植物仅为细辛属植物辽     

虎凤蝶属雄性外生殖器超微结构的比较（鳞翅目：凤蝶科）

运用扫描电镜观察了虎凤蝶属现有4种雄成虫的外生殖器。结果表明：中华虎凤蝶Lueh-dorfia chinensis Leech 、长尾虎凤蝶L. longicaudata Lee、乌苏里虎凤蝶L. puziloi Erschoff和日本虎凤蝶L. japonica Leech雄性外生殖器的一般形态结构相似,而其抱器、钩状突、阳茎、阳茎轭片的超微结构存在着差异,这些特征可作为鉴定的依据。通过对雄性外生殖器形态结构的比较,以及有关结构参数的聚类分析,讨论了4种虎凤蝶的亲缘关系。作者认为,中华虎凤蝶具有最原始的结构特征,可能较接近该属祖先,长尾虎凤蝶则与其较近缘;乌苏里虎凤蝶与日本虎凤蝶相对较近缘,与前两种差异略大。     

珍稀濒危昆虫——中华虎凤蝶的生物学

中华虎凤蝶(Luehdorfia chinensis Leech)在杭州一年发生一代,以蛹越夏、越冬.1987—1989年,卵见于3月中旬至4月上、中旬,幼虫发生于4月上甸至5月中旬.在喂食25%蜂蜜水的条件下,雌、雄蝶寿命分别为12.9±5.82天和11.5±6.64天.卵2—35粒一堆,产在寄主叶背.卵期23.1±8.32天,卵发育起点温度7.68℃,有效积温111.40目度.幼虫期平均36.3天,全幼虫期取食叶面积25362.00±1820.68mm².蛹期307.5±4.65天.本文并就该蝶发生数量少的原因和应采取的保护措施作了简要讨论.     

中华麝凤蝶生物学特性研究

以野外观察、实验地饲养等方法, 详细记述了中华麝凤蝶 Byasa confusa (Rothschild)各虫态的形态特征、生活史和习性等生物学特性。在南京地区该蝶1 年发生2 代, 幼虫5 龄, 以绵毛马兜铃Aristolochia mollissima 为食, 卵期8-10 d, 幼虫期23-29 d。老熟幼虫在枝条上化蛹。该蝶以蛹滞育越冬。第一代成虫发生高峰期为4 月中旬至5月中旬; 第二代成虫发生高峰期在7 月下旬到9 月上旬, 存在世代重叠现象。     

温度对黄粉虫幼虫生长发育及体液免疫防御能力的影响

【目的】探究饲养温度对黄粉虫Tenebrio molitor幼虫生长发育和体液免疫防御的影响。【方法】测定了不同温度（18, 22, 26和30℃）下饲养的黄粉虫幼虫的发育历期、蛹重、化蛹率;采用抑制区分析法测定了不同温度下饲养的免疫（用生理盐水将大肠杆菌Escherichia coli配制成1×104个菌体/μL悬浮液,用微量注射器将其注入虫体腹部的背面,每头幼虫注射1 μL）和非免疫(注射生理盐水)黄粉虫幼虫血淋巴的抑菌和溶菌酶活性,通过分光光度法测定了其酚氧化酶活性。【结果】结果显示,黄粉虫幼虫发育历期随饲养温度的上升而明显缩短（P<0.0001）,而不同温度下蛹重（P=0.067）与化蛹率（P=0.869）差异不显著。免疫组黄粉虫幼虫血淋巴的抑菌、酚氧化酶和溶菌酶活性随饲养温度上升而降低：抑菌和酚氧化酶活性随温度变化差异极显著（P<0.0001）,溶菌酶活性差异显著（P=0.013）。【结论】本研究结果表明,温度对黄粉虫的生长发育和免疫防御具有较大的影响,低温下黄粉虫幼虫的发育历期延长,但其体液免疫防御能力明显增强。     

温度对海洋底栖端足类日本大螯蜚(Grandi-dierella japonica)存活、生长和发育的影响

日本大螯蜚（ Ｇｒａｎｄｉｄｉｅｒｅｌｌａ ｊａｐ ｏｎｉｃａ）生长发育的适温范围为 ２０～２６℃。不同发育期耐受温度范围不同,刚孵化幼体温度下限为１１℃,上限为３２℃,以后随着幼体发育,其对低温的适应力逐渐增强。雄性个体对极限温度的忍耐力低于雌性。在耐受温度范围内,幼体的生长发育随着温度的提高而加快。研究结果表明,日本大螯蜚实验室培养温度宜选择在２０～２６℃,用其进行的沉积物急性和慢性毒性生物检验的实验温度均宜选择在 ２０℃。     

Effects of temperature on developmental performance, survival and growth of sea lamprey embryos

This study assesses the influence of thermal regime on the development, survival rates and early growth of embryos of sea lamprey Petromyzon marinus incubated at five constant temperatures (7, 11, 15, 19 and 23° C). The time from fertilization to 50% hatching and from hatching to 50% burrowing were inversely related to incubation temperature. All the embryos incubated at 7° C died at very early stages, while those maintained at 11° C did not attain the burrowing stage. Survival from fertilization to hatching was 61, 89, 91 and 89% at 11, 15, 19 and 23° C, decreasing to 58, 70 and 70% from hatching to burrowing at 15, 19 and 23° C, respectively. Larvae reared during the first 3 months of exogenous feeding in a common environment at constant 21° C, revealed maximum survival for an incubation temperature of 15° C (43% of burrowed larvae) decreasing strongly at 19° C (16%) and 23° C (one suvivor among 240 larvae). Body length at the burrowing stage was maximum for embryos incubated at 19° C, but body mass increased in the interval 15–23° C. Mean incubation temperatures experienced by 117 broods during the embryonic development in the source river were estimated in 15·3±2·30° C and 16·7±1·76° C (mean±1 s.d .) for the periods fertilization-to-hatching and hatching-to burrowing, respectively.     

幼虫期短时高温暴露对二点委夜蛾存活和繁殖的影响

【目的】随着全球气候变暖,夏季短时极端高温发生的频率逐渐增加。本研究旨在探明二点委夜蛾Athetis lepigone幼虫期对高温的适应性。【方法】将二点委夜蛾不同日龄(1,6,12和18日龄)幼虫在不同高温(35,38和41℃)条件下暴露不同时间(0.5,1,2,4和6 h)后转移至适温(26℃)继续饲养,观察短时高温对其存活率、发育历期、化蛹率、羽化率、雌虫寿命、单雌产卵量及次代卵孵化率的影响。【结果】幼虫期短时高温暴露的温度和时间对二点委夜蛾幼虫的存活率和发育历期有显著影响,而对化蛹率、成虫羽化率、雌虫寿命、单雌产卵量以及次代卵孵化率影响不显著。随着温度的升高和处理时间的延长,幼虫存活率逐渐降低,发育历期逐渐延长。其中,18日龄的幼虫最为敏感,38℃和41℃暴露6 h后存活率分别为58.3%和17.7%,显著低于对照,发育历期分别为25.5 d和29.2 d,较对照显著延长。【结论】幼虫期经历短时高温暴露仅对幼虫的存活和发育历期有影响,而对后续蛹和成虫的生长发育及成虫繁殖力没有影响。     

低温和饥饿对华贵栉孔扇贝幼虫生长和存活的影响

为了弄清我国南方低温季节能否利用自然水温进行华贵栉孔扇贝人工育苗以及饵料缺乏对幼虫的影响,于2008年10月上旬和11月下旬,分别在水温25.5—28.0℃和18.2—22.5℃条件下,研究了低温和饥饿对幼虫生长、存活的影响。实验分两次设置常温、低温和饥饿3个组进行。结果表明,低温情况下,幼虫摄食较少,活力差、绝大部分沉入水底,生长缓慢,发育迟缓,但存活率仍较高;饥饿不但抑制幼虫的生长和发育,同时也显著地降低幼虫的存活率。此外,低温和饥饿的结合会加剧对幼虫生长、发育、存活等的抑制作用。这些结果说明在我国南方水温低于23℃的季节利用自然水温已不适合进行华贵栉孔扇贝苗种生产。     

The effect of temperature on the growth,development and survival of Macropetasma africanus (Balss) (Penaeoidea:Penaeidae) larvae reared in the laboratory

Macropetasma africanus (Balss) has been successfully spawned and its larvae reared under controlled laboratory conditions. The relationship between egg number (E) and female total length (L) was E = 18.59 L^2.11. An experiment was designed to test the effect of temperature on larval development, survival and growth. Temperature effected larval development time, from 13–15 days at 25°C, to 25 days at 15°C (nauplius 1 to post-larva). Mortality was low for the naupliar stages at 25, 22 and 18°C, while at 15°C only 52% of the larvae reached nauplius 6. Mortality was highest from nauplius 6 to protozoea 1 (17, 21, and 18% at 25, 22, and 18°C, respectively), but decreased considerably for all temperatures once the mysis stage was reached. Overall survival rates from nauplius 1 to post-larva decreased with decreasing temperature (65, 54, 48, and 39% at 25, 22, 18, and 15°C respectively). Temperature also significantly affected larval growth. At 25°C mean total length was significantly (P < 0.05) larger than at 15°C (protozoea 2 to post-larva), while from protozoea 3 to post-larva total length differences were significantly different (P < 0.05) between 18 and 25°C. M. africanus has a major spawning peak in summer, suggesting that there may be a selective advantage to reproducing during the warmer months.     

Effects of temperature during early life history on embryonic and larval development and growth in haddock

The effect of incubation temperature (2, 4, 6, 8 and 10° C) on haddock Melanogrammus aeglefinus development and growth during the embryonic period and in subsequent ontogeny in a common post‐hatch thermal environment (6° C) was investigated. Hatching times were inversely proportional to incubation temperature and ranged from 20·3 days at 2° C to 9·1 days at 10° C. Growth rates were directly proportional to incubation temperature during both the embryonic and larval periods. There was a significant decline in growth rates following hatch in all temperature groups. Compared to the endogenously feeding embryos, growth rates in the exogenous period declined by 4·4‐fold at 4° C to 3·9‐fold at 8° C, indicative of the demarcation between the endogenous and exogenous feeding periods. Yolk utilization varied from 17 days at 2° C to 6 days at 10° C and followed a three‐stage sigmoidal pattern with the initial lag period inversely proportional to incubation temperature. Time to 50% yolk depletion varied inversely with temperature but occurred 1–1·5 days post‐hatch at all temperatures. Additionally, the period between 10 and 90% yolk depletion also decreased with increased temperature. Overall developmental rate was sequential with and directly proportional (2·3‐fold increase) to incubation temperature while the time spent in each developmental stage was inversely proportional to temperature. Larger embryos tended to be produced at lower temperatures but this pattern reversed following hatch, as larvae from higher temperature groups grew more rapidly than those from other temperature groups. Larvae from all temperatures achieved a similar length (c.total length 4·5 mm) upon complete yolk absorption. The study demonstrated the significant impact that temperature has upon developmental and growth rates in both endogenous and exogenous feeding periods. It also illustrated that temperature changes during embryogenesis had significant and persistent effects on growth in subsequent ontogeny.     

环境温度对马尾松毛虫发育与存活的影响

通过模拟马尾松毛虫2、3代发生区内第2代幼虫发生期温度的变化,进行了高温、常温和低温3组变温试验.结果表明,在相同光照条件下,3龄以前的马尾松毛虫幼虫死亡率明显不同.马尾松毛虫幼虫死亡率在长光周处理内低温组为25.55%,常温组为55.13%,高温组为58.23%;在短光周处理内低温组为32.67%,常温组为64.67%,高温组为94.32%,说明高温是影响马尾松毛虫低龄幼虫死亡的主要原因.高温还影响马尾松毛虫幼虫的滞育.在相同短光周条件下,幼虫孵出后20 d,高温组幼虫40%发育为5龄,而低温组和常温组全部滞育;幼虫孵出后48 d,高温组全部结茧,而低温组和常温组仍全部滞育.试验证明,马尾松毛虫在第2代幼虫孵出后20 d内如遇连续高温环境,即使在短光周条件下,幼虫也不会滞育.     

不同温度条件下土壤水分对羊草幼苗生长特性的影响

采用生长箱控制方法,研究了羊草幼苗生长对5个温度和5个水分梯度的响应。结果表明,不同温度改变了羊草生物量对土壤水分变化的响应类型。在20～26℃下羊草植株生物量对土壤水分的响应曲线呈三次多项式或抛物线变化规律,而在29～32℃下为指数方程。在温度较低或适度时,轻度乃至中度干旱有促进生长的作用,但在温度较高时轻度干旱及比其程度更高的干旱显著地影响羊草的生长,表明羊草在较高温度下对水分更加敏感。在适当的温度下(26℃),羊草根的贡献率或根冠比与土壤水分呈直线关系。高温加强了干旱对羊草幼苗生长的抑制作用,表明高温降低了羊草对干旱的适应能力。     

温度对大猿叶虫发育、存活和繁殖的影响

在光周期14L:10D、75%RH的条件下研究不同温度对大猿叶虫Colaphellus bowringi Baly生长发育、存活率和繁殖的影响。结果表明,卵、幼虫和蛹的发育起点温度分别为11·86,11·17和10·15℃,有效积温分别为61·6,110·8和65·3日·度;22℃时卵的孵化率和蛹的羽化率最高,分别达96·04%和94·26%;滞育后成虫寿命雌虫普遍长于雄虫,25℃下的产卵期11～34d,每雌产卵量平均861粒,最高达1527粒。     

盐度波动对中国对虾稚虾蜕皮、生长和能量收支的影响

采用实验生态学方法研究了在盐度为20的条件下,4个盐度波动幅度（2、4、6、8）对中国对虾稚虾蜕皮和生长的影响.结果表明：中国对虾的蜕皮率为13.3%～15.4%,处理间差异未达到显著水平;盐度波动幅度为4的情况下,对虾的特定生长率最大,用在生长上的能量最高,用于呼吸的能量最低,生长迅速;盐度波动幅度为2的情况下,中国对虾的摄食量最低;盐度波动幅度为2和4的情况下,对虾的食物转化效率最高;不同处理中国对虾用在蜕皮上的能量差异不显著.盐度波动幅度过大不利于中国对虾稚虾的生长,但对蜕皮无影响.