胡瓜钝绥螨捕食茶橙瘿螨的实验种群生命表及捕食作用初探

本在25℃条件下初步研究了胡瓜钝绥螨捕食茶橙瘿螨的实验种群生命表、各螨态取食量及猎物－－卵转化率。25℃时胡瓜钝绥螨的净增殖率R0＝21．7862,世代平均周期T＝16．1822,内禀增长率rm＝0．1904,周限增长率λ＝1．2097,种群倍增所需时间t＝3．6405。日平均产卵量2．19粒／天,总产卵量36－48粒／雌,平均38．97粒／雌。胡瓜钝绥螨雌螨－生取食量1978．49头。雄螨取食量879．56头。猎物：卵转化率为79．78头茶橙瘿螨：2．19粒胡瓜钝绥螨卵。     

棕榈蓟马在茄子上的种群增长、分布和抽样技术研究

棕榈蓟马在茄子上的种群增长,用种群增长模型来分析,露地栽培的成虫、若虫种群增长率ｒ分别为０．０６３０和０．０８０１,设施栽培分别为０．０９８３和０．１０３６。设施栽培的逻辑斯蒂曲线的Ｋ值为３３．９０,明显大于露地栽培的Ｋ值２３．５０。棕榈蓟马种群在茄子上空间分布调查结果,成、若虫的Ｍ＾＊－Ｍ回归式分别为Ｍ＝０．６０１１＋１．４６８Ｍ和Ｍ＾＊＝７．２５１５＋２．０６４０Ｍ。成虫＋若虫的Ｍ－Ｍ回归式为     

一类害虫与天敌模型的振动性

1．引言1963年F.E.Smith在VerhulSt-pear工作的基础上认为种群的实际增长率不是种群的内禀自然增长率,在资源和生存空间有限的环境中,种群的增长率总存在一个上限k．当种群的密度N(t)和种群的增长速度N(t)的ρ倍之和逐渐向着上限上升时,实际增长率就要减少,因而提出如下模型其中可为种群的内禀自然增长率,k为环境容纳量,N（t）为种群在时刻t的密度（或数量）．（1）中调节因子op所引起的调节效应,多数情况下会有某种时滞,也就是说种群的增长率不仅与时刻t的种群密度有关而且还与以前的时间,;的种群密度有关,于是（1）式加滞…     

湖北石首麇鹿国家级自然保护区麇鹿种群动态

为实现麇鹿回归大自然的目标,1993年和1994年,湖北石首麋鹿国家级自然保护区（以下简称石首麋鹿保护区）分别从北京麋鹿苑引入麋鹿30头（8♂,22♀）和34头（10♂,24♀）建立了繁殖种群。自2000年6月开始,作者每月一次（7—10d）实地监测石首麇鹿保护区内、外的麋鹿种群动态。到2006年产仔季节结束后,该保护区内的麋鹿种群达522头,2006年产仔前性比为1：1．22。用指数增长模型拟合种群增长曲线,1998年后石首麋鹿保护区内的麋鹿种群呈指数增长（Nt=84e^0.226t）,其瞬时增长率为0．226;1998年夏季长江暴发特大洪灾,石首麇鹿保护区内的部分麋鹿逃逸到长江南岸,形成了自然野化麋鹿种群。该自然野化种群比保护区内麇鹿种群增长快,其瞬时增长率达到0．267。湖北石首和江苏大丰两个国家级自然保护区内麋鹿种群的出生率和增长率差异显著,而两地的死亡率无显著差异。石首麋鹿保护区内的麋鹿种群年均出生率（26．8％,P=0．010）和年均增长率（21．7％,P=0．038）均显著地高于江苏大丰国家级自然保护区内麇鹿种群的年均出生率（21．6％）和年均增长率（17．0％）。由于生境退化和人为干扰,当前石首麋鹿保护区内的麋鹿种群增长已开始出现密度制约迹象,亟待采取有效措施来改善麋鹿的生存繁衍条件[动物学报53（6）：947—952,2007]。     

标志技术在研究小皱蝽成虫种群特征中的应用

应用标志－释放－回收技术研究小皱蝽成虫的主要种群特征,结果如下：（１）成虫扩散的偏离度Ｋｕ＝２．４,为一阶峻开曲线;（２）分别用Ｐｅｔｅｒｓｏｎ和Ｊａｃｋｓｏｎ方法对种群蜜度进行了估计,结果表明,Ｊａｃｋｓｏｎ的方法较好;（３）雄虫平均寿命４０－４５,虫平均寿命１２０－１３０。天。     

广州地区自然条件下扶桑绵粉蚧入侵定殖能力研究

【背景】扶桑绵粉蚧是一种对棉花等作物具有严重威胁的新的外来人侵害虫,2008年8月在广州市区扶桑上发现该虫。关于该虫入侵种群的大小是需要明确的基本人侵生物学问题之一。【方法】采用了野外接虫、定点系统跟踪观察的方法,研究了广州地区番茄、棉花田间扶桑绵粉蚧的最小入侵种群规模。【结果】扶桑绵粉蚧初始种群侵入棉花、番茄田3d后数量急剧下降,分别减少了82．7％、61．2％,进入3龄后田间种群数量呈现持续小幅度减少的规律,进入产卵期的雌虫出现概率分别为2．83％、2．5％。棉花上扶桑绵粉蚧单雌产卵量为532．6粒,明显高于番茄（418．4粒）。棉花、番茄田的入侵种群趋势指数分别为15．09、10．46,下一代种群呈明显增长趋势,能够成功定殖。棉花、番茄田扶桑绵粉蚧自然种群存活曲线均符合Ⅰ型（凹型）,存活率（S）与接虫后天数（D）的关系模型分别为S=（1．0000＋1．1．505D）-1.1250,S=（Q9996＋Q124810）^-3.0614。根据进入产卵期雌虫的概率,计算出保证扶桑绵粉蚧成功入侵的最小自然种群规模为36—40头。【结论与意义】广州地区6～8月番茄、棉花田新人侵的扶桑绵粉蚧自然种群存活曲线为Ⅰ型（凹型）,最小入侵种群规模为36—40头。该结果为深入研究扶桑绵粉蚧的入侵生物学特性和制定防治策略等提供了依据。     

三个家猪品种和rob易位群染色体分带多态性的比较

对家猪不同品种及家系间的染色体组型、C－带、Ag－NORs多态性进行的研究表明：杜洛克猪、约克夏猪、长白猪体细胞染色体数2n＝38,核型2n＝10sm＋12m＋4st＋12t,而13／17易位纳合子猪（36,rob．13／17）的体细胞染色体数2n＝36,核型2n＝10sm＋12m＋6st＋8t;13／17易位杂合子猪（37,rob．13／17）的体细胞染色体数目为2n＝37,核型为2n＝10sm＋12m＋5st＋10t。5种家猪的C－带在13～18号染色体上存在大、中、小三种类型,且呈多态性分布。杜洛克猪、约克夏猪、长白猪、13／17易位纳合子猪、13／17易位杂合子猪的Ag－NORs均数分别为2．05、2．062．00、1．99、1．98,说明Ag－NORs在品种、个体及细胞间具有多态性.     

南美斑潜蝇为害大棚芹菜和芸豆的产量损失测定及经济阈值分析

研究结果表明：①南美斑潜蝇为害大棚芹菜和芸豆,其虫道面积和产量呈负相关,与产量损失率呈正相关;②曲线回归方程为：Y（大棚芹菜产量）＝4．233／（1＋0．2669e0.0281X）,Y（大棚芸豆产量）＝500950．702／（1＋39262,76541e^0.0103X）,Y（大棚芹菜产量损失率）＝68．075／（1＋23．1517e^-0.071X）,Y（大棚芹菜产量损失率）＝71．765／（1＋4．26245e^-0.0305X）;③经济阈值模型为：X（大棚芹菜）＝14．0845ln[23.1575L/(68.075-L)],X(大棚芸豆）＝27．3973ln[4.26245L/(71.765-l)]。     

芫荽花再生植株及离体快速繁殖

1植物名称芜萎（Coriandrumsativum）,又名胡美,俗称香菜。2材料类别幼嫩花蕾和幼芽。花蕾取自新乡郊区菜园内,刚出现一个花蕾的芜萎苗。幼芽取自本校菜市场的芜萎幼苗。3培养条件花蕾诱导愈伤组织培养基：门）MS＋2,4～D2．omg·t－‘（单位下同）＋6－BAO．3＋NAAO．2;（2）MS＋2,4－－D0．2＋6－BA0．2＋NAA2．0;（3）MS＋2,4－－DI．0＋6－BA0．5＋KT0．2;（4）MS＋6－BA0．7＋NAAI．5＋KT0．1;（5）MS＋2,4－－DI,5十6－BA0．7＋NAA0．2;（6）MS＋2,4－－D0．4十NAAI．0＋KT0．工。芽分化培养基：…     

种群增长的分段指数模型及其参数估计

本文给出了种群增长的分段指数模型其中N（t）是在时刻t种群的密度,No=N（t0）,r0和rl是群群的内禀增长率,t0是转变点,H（t-t0）=1,t≥t0,H（t-t0）=0,t＜t0．利用非线性模型的正割法（DUD,Doesn’tusederivatives）,可同时确定模型的所有参数（包括交点t0在内）．并用于描述长爪沙鼠种群动态．     

梨小食心虫自然种群与室内继代饲养种群生物学特性比较

【目的】为明确梨小食心虫Grapholita molesta自然种群与室内继代饲养种群生物学特性的差异, 以期为梨小食心虫的人工饲养以及测报与防治提供理论依据。【方法】本研究对室内继代饲养的和从田间采集的梨小食心虫, 在室内同等条件下饲养, 较系统地观察两者的生物学特性并对其主要生命表参数进行了比较。【结果】在本试验条件下, 梨小食心虫室内继代饲养种群的蛹期极显著长于自然种群（t=-10.78, df=4, P=0.0004）; 卵期、 幼虫期以及预蛹期均稍长于自然种群, 但无显著差异。室内继代饲养种群的幼虫存活率、 化蛹率、 羽化率极显著高于自然种群（存活率： t=-7.61, df=4, P=0.0016; 化蛹率： t=-24.32, df=4, P=0.0017; 羽化率： t=-6.96, df=4, P=0.0022）; 两个种群的卵孵化率、 蛹重、 成虫寿命、 产卵前期、 产卵期及单雌产卵量均无显著差异。自然种群蛀果率高于室内继代饲养种群, 但差异不显著。生命表分析表明, 梨小食心虫室内继代饲养种群的种群趋势指数I、 净增殖率R₀、 内禀增长率r_m、 平均世代周期T、 周限增长率λ均极显著高于自然种群（I： t=-12.20, df=4, P=0.0003; R₀： t=-11.72, df=4, P=0.0003; r_m： t=-9.77, df=4, P=0.0006; T： t=-12.05, df=4, P=0.0003; λ： t=-9.79, df=4, P=0.0006）, 种群加倍时间Dt极显著低于自然种群（t=7.17, df=4, P=0.0020）。【结论】室内继代饲养种群在室内连续饲养50多代后, 与自然种群比较, 不仅各生命表参数和钻蛀危害果实的能力没有下降, 反而在与自然种群同等的室内饲养条件下, 表现了更好的适应性, 在本供试条件下, 后代具有更大的种群增长潜力。所以, 利用室内继代饲养种群进行的相关试验研究结果可以作为梨小食心虫预测预报与防治实践的依据。     

Construction of population growth equations in the presence of viability constraints

A mathematical method based on the G-projection of differential inclusions is used to construct dynamical models of population biology. We suppose that the system under study, not being limited by resources, may be described by a control system

李肖叶甲成虫数量及三维空间格局动态

对合肥地区李肖叶甲成虫数量动态及三维空间格局进行研究,结果表明该成虫5月下旬初见,6月4日至7月16日为发生高峰期,9月上旬仍有零星虫口。6月4日至9月10日种群增长模型为y=1692.2258e-0.0545t,6月4日至8月27日树冠上部部位增长模型为y=205.60e-0.0523t,树冠西部部位的增长模型为y=257.13e-0.0505t。样地中的李肖叶甲5月21日至8月13日半变异函数方程是y=0.0709x3-10.479x2+391.67x-300.71、y=-0.0122x3+1.1201x2-19.781x+317.84、y=-0.0013x3+0.1613x2-4.4862x+67.363、y=-0.0016x3+0.9177x2-11.495x+551.94、y=-0.0029x3+0.3034x2-7.5906x+103.37和y=-0.0002x3+0.0172x2-0.4975x+13.691,变程在20.3938—65.0289之间,均为聚集格局,聚集强度指标表明也均为聚集格局;树冠东、西、南、北方位的水平分布5月21日至8月13日的C值均大于1,I值均大于0,CA值均大于0,Iw值均大于1,为聚集格局;树冠上、中、下方位的垂直分布6月4日至8月13日的C值均大于1,I值均大于0,CA值均大于0,Iw值均大于1,为聚集格局;5月21日至8月13日的树冠东、南、西、北、上、中、下部位的C值均大于1,I值均大于0,CA值均大于0,Iw值均大于1,三维分布均为聚集格局。用Iwao公式计算的结果与聚集强度指标分析的结果一致。6月4日—8月13日林间李肖叶甲的种群聚集均数λ值均大于2,聚集是李肖叶甲本身的行为所致。     

黑线仓鼠种群数量动态预测研究

１９８４－１９９１年３－１０月,每月中旬在中国农科院草原研究所试验场的不同牧草和作物地进行调查,１９８４－１９９１年共捕获鼠４０９３只,其中黑线仓鼠２９２０只占７１．３４％。黑线仓鼠种群数量季节和年度变化明显,利用电子计算机对黑线仓鼠种数量进行分析,提出种群数量繁殖指数和动态模型以及短、中、长期预测公式、预测准确率为９０．０％。并对影响种群数量的因素进行了初步分析。     

大型溞生长、生殖和种群增长的研究

年龄6±6小时的纯系大型溞培养在25±1℃静置换水条件下,饲以斜生栅藻,其平均寿命为68.40±9.82天。龄期(x)和年龄(t,天)之间呈曲线迴归关系:t=-2.245+1.510x+0.035x2(r=0.99,p3.86-0.131t)(式中Y为累计生殖量个数,t为天数)。       

Life History of Black Seabream, Spondyliosoma cantharus, off the Canary Islands, Central-east Atlantic

Black seabream, Spondyliosoma cantharus, caught off the Canary Islands is characterized by a protogynous hermaphroditism. The size range of the catches is between 8 and 40cm, with a main distribution between 16 and 24cm. The mean length of the individuals shows an increase with increasing depth. Males:females ratio is unbalanced in favour of females (1:2.18). The reproductive season extends from late autumn to mid spring, with a peak in spawning activity in January–February. A dichromatism is found between males and females during the spawning season. Males reach maturity at a larger total length, 22.7cm (3 years old), than females, 17.3cm (2 years old). Morphometric relationship between length and mass for the whole population is described by the parameters: a=0.00732, and b=3.24747. Otoliths age readings indicate that the exploited population consists of eleven age groups (0–X years), including a very high proportion of individuals between 2 and 3 years old. The von Bertalanffy growth parameters for the whole population are: L=43.35cm, k=0.24 year–1, and t0=–0.11 year. The rates of total, natural and fishing mortality are 1.36, 0.52 and 0.84 year–1, respectively. The length at first capture is 16.8cm. The exploitation rate indicates that the stock is overfished.     

Transposition induction of the mobile genetic element Dm412 in the Drosophila genome using heat shock]

Males of Drosophila melanogaster isogenic line with oligogene mutation radius incompletus (ri) were exposed to standard heat-shock (SHS: t = 37 degrees C, 90 min) and heavy heat-shock (SHS: three-fold transfer of males from t = 37 degrees C, 2h, t0t = 4 degrees C 1 h, and back). At F1 of the treated males with untreated females of the same isogenic line mass transpositions of MGE Dm412 were found. The new positions of MGE seem to be not random, and 5 "hot sites" of transpositions were detected. The probabilities of transpositions were estimated after SHS and HHS and in control sample. They were, correspondingly, 3.4 x 10(-2), 8.7 x 10(-2) and less than 4.1 x 10(-4) transpositions per genome, per site occupied, per generation. Therefore, as a result of HS treatment, the probabilities of transpositions were two orders of magnitude increased as compared to control, directly at next generation after induction. Comparison of these results with those obtained after step-wise temperature treatment shows that induction is dependent rather of "stressor effect" of temperature treatment than of treatment way used.     

Microbial production of natural δ-decalactone and δ-dodecalactone from the corresponding α,β-unsaturated lactones in Massoi bark oil

Summary The hydrogenation of ,-unsaturated Massoi lactones to natural -lactones by various microorganisms belonging to the Basidiomycetes and by Saccharomyces ce cerevisiae has been studied. Natural -decalactone is an important constituent of several natural flavourings. Process parameters for the hydrogenation by baker's yeast have been characterized on a 2-1 fermentation scale. High hydrogenation activity by baker's yeast was observed at pH 5.5, a temperature of 35° C, no oxygen limitation and constant addition of glucose. By stepwise addition of 2-decen-5-olide about 1.2 g/l of 5-decanolide could be obtained in a fermentation of 16 h. The same concentration could be obtained in 8 h by adding all the substrate at once (1.7 g/l) in the presence of 2% cyclodextrin.Offprint requests to: P. H. van der Schaft     

The kinetics of hydrogen photoproduction by adapted Scenedesmus

Summary In our earlier work we have shown that hydrogen photoproduction by photosystem I of Scenedesmus does not require O₂ evolution or cyclic photophosphorylation but must be due to non-cyclic electron flow from organic substrate(s) through photosystem I to hydrogenase, where molecular H₂ is released. The kinetics of this reaction are rather complex, in that H₂ photoproduction by Scenedesmus evidently occurs in two phases: a rapid initial phase which depends upon the dehydrogenation of a pool of H donors, and a later and slower second phase which is limited by the flow of electrons from fermentation. When adapted cells were incubated in the dark with an inhibitor (Cl-CCP or salicylaldoxime), the pool utilized by photosystem I gradually disappeared. However, the pool gave a rapid rate of hydrogen photoproduction when the adapted cells were illuminated immediately after adding the inhibitor. The rate at which the pool was utilized depended upon the light intensity and was not light-saturated at the highest intensity tested (3.4×10³ W cm^-2).With light of at least medium intensity (1.67×10³ W cm^-2), the pool was rapidly exhausted and the reaction became dependent upon the leak of electrons from fermentation. The size of the leak was found to depend upon the level of reduced organic compounds in the cell, since this process was depressed by starving the cells and was much enhanced by adding glucose or by growing the cells heterotrophically. A quantitative relationship was found between the amount of glucose added and the resulting stimulation of H₂ photoproduction, in that one mole of glucose gave about 0.5 mole of H₂ gas.The following abbreviations were used: Cl-CCP=carbonyl cyanide m-chlorophenylhydrazone; DCMU=3-(3,4-dichlorophenyl)-1,1-dimethylurea; DCPIP=dichlorophenol-indophenol; PS=photosystem.These studies were supported by contract No. AT-(40-1)-2687 from the U. S. Atomic Energy Commission.     

Mathematical description of stress relaxation of bovine femoral cortical bone

In 1993 we proposed an empirical formula for describing the relaxation modulus of cortical bone based on the results of stress relaxation experiments performed for 1 x 10(5) sec: [E(t) = E0{A exp[ -(t/tau1)beta] + (1 - A) exp(-t/tau2)}, (0 < A, beta <1 and tau1 < tau2) where E0 is the initial value of the relaxation modulus, A is the portion of the first term, tau1 and tau2 are characteristic relaxation times, and beta is a shape factor [Sasaki et al., J. Biomechanics 26 (1993), 1369]. Although the relaxation properties of bone under various external conditions were described well by the above equation, recent experimental results have indicated some limitations in its application. In order to construct an empirical formula for the relaxation modulus of cortical bone that has a high degree of completeness, stress relaxation experiments were performed for 6 x 10(5) seconds. The second term in the equation was determined as an apparently linear portion in a log E(t) vs t plot at t>1 x 10(4) sec. The same plot for experiments performed for 6 x 10(5) seconds revealed that the linear portion corresponding to the second term was in fact a curve with a large radius of curvature. On the basis of this fact, we proposed a second improved empirical equation E(t) = E0{A exp [ -(t/tau1)beta] + (1 - A) exp[-(t/tau2)gamma]}, (0相似文献