安徽滁州雌性丽斑麻蜥繁殖特征

在安徽滁州地区丽斑麻蜥(Eremias argus)年产两窝卵。窝卵数及窝卵重与雌体体长呈正相关,相对窝卵重与雌体体长无关,卵重与窝卵数无关。窝卵数、窝卵重及卵重在窝序间无明显的差异。卵长径与卵短径呈正相关,卵长径与窝卵数呈负相关,而卵短径与窝卵数无关。雌体主要通过增加窝卵数增加繁殖输出。     

山地麻蜥的雌性繁殖和孵出幼体特征

山地麻蜥年产多窝卵。窝卵数、窝卵重和卵重与雌体体长呈正相关,卵重与窝卵数无关。窝卵数、窝卵重和卵重不存在明显的季节变化。卵长径与卵短径呈正相关,卵长径、卵短径与窝卵数无关。雌体通过增加窝卵数和卵大小增加繁殖输出。孵出幼体的体重、体长、尾长、躯干干重、刺余卵黄不存在季节差异,但5月份孵出幼体的脂肪体高于4月份。     

卵跳小蜂Ooencyrtus nezarae Ishii对豆缘蝽和豆璧蝽卵的选择性和密度反应(英文)

本文研究了卵跳小蜂对豆缘蝽 (R .clavatusThunberg)和豆璧蝽 (P .hybneriGmelin)卵的选择性和密度反应。在自由选择试验中 ,两种豆蝽卵中羽化的卵跳小蜂在不同的卵密度和比例中均选择豆缘蝽 ;而在非选择性试验中 ,从豆璧蝽中羽化的卵跳小蜂同时选择豆缘蝽和豆璧蝽卵 ,寄生率较高 ;然而 ,从豆缘蝽卵羽化的卵跳小蜂对豆璧蝽卵的寄生率非常低。嗅觉试验表明 ,从豆缘蝽卵上释放的气味对卵跳小蜂的搜寻和寄生行为影响很大。卵跳小蜂寄生的卵数量随着豆缘蝽和豆璧蝽卵密度的增加而提高 ;然而 ,卵跳小蜂对豆璧蝽的寄生率随着卵的密度增加而降低 ,尤其是从豆缘蝽卵中羽化的寄生蜂。研究还表明 ,卵跳小蜂在大田中对豆缘蝽卵的寄生存在着空间或时间上的障碍。     

皮纹学分析对两组三胞胎卵性诊断的研究

本文以皮纹学指标分析了两组三胞胎的卵性诊断问题。结果表明,指纹类型的差异性,同卵为15％,异卵为60％,十指纹型双手对应性差异,同卵为20％,异卵在55％以上。三胞胎不论同卵还是异卵,比起双胞胎的同卵或异卵,皮纹参数的差异要大一些。     

浙江舟山五种卵生游蛇科动物个体大小、窝卵数和卵大小之间的关系

阐明五种游蛇科动物雌体大小、窝卵数和卵大小之间的关系和雌性繁殖特征的种间差异。５种蛇均产单窝卵,产卵高峰期为６月下旬至７月,窝卵数与雌体大小（ＳＶＬ）呈显著的正相关,相对窝卵重与雌体ＳＶＬ无关,卵理与窝卵数无关。灰鼠蛇卵重与雌体ＳＶＬ呈正相关,赤链蛇、王锦蛇、黑眉锦蛇和乌梢蛇的卵重与雌体ＳＶＬ无关,黑眉锦蛇卵长径与窝卵娄呈负相关,其余４种蛇卵长径与窝卵数无关。５种蛇卵长径与短径无关。黑眉锦蛇卵短径     

皮纹学分析对两组三胞胎卵性诊断的研究

本文以皮纹学指标分析了两组三胞胎的卵性诊断间题。结果表明,指纹类型的差异性,同卵为 15%,异卵为60%,＋指纹型双手对应性差异,同卵为20%,异卵在”％ 以上。三胞胎不论同卵还 是异卵,比起双胞胎的同卵或异卵,皮纹参数的差异要大一些。     

田间转Bt基因水稻上稻飞虱卵量、孵化率及天敌作用

为了评估转基因水稻释放后对非靶标害虫及其天敌的影响, 本研究在浙江大学实验农场和中国水稻研究所实验农场2008和2009年连续两年监测了转Bt基因水稻对田间稻飞虱着卵量、卵孵化率、卵被捕食率、卵被寄生率和卵死亡率的影响。结果表明: 两年2个调查地点3个水稻品系（克螟稻1、克螟稻2和秀水11）上的稻飞虱平均每分蘖着卵量、卵孵化率、卵被捕食率和卵被寄生率的趋势基本一致, 而且田间3个水稻品系上稻飞虱卵量的高峰期均持续2周左右; 但是两年2个调查地点3个水稻品系上稻飞虱卵死亡率则没有一致的趋势。此外, 总体上3个水稻品系上稻飞虱平均每分蘖着卵量、卵孵化率、卵被捕食率、卵被寄生率和卵死亡率差异均不显著（P>0.05）。因此, 稻田中转Bt基因水稻对稻飞虱卵没有显著的影响。     

新疆石河子棉蚜越冬卵的发育规律

棉蚜雌性蚜交配个体平均产卵量为 6 3± 1 1粒 ;未交配个体也产卵 ,卵亦变色 ,但卵量极少。越冬卵经 5 %NaOH浸泡 2 4h后卵壳透明 ,镜下观察可见受精卵胚胎发育到体躯分节期开始越冬。冬后胚胎发育仅处在颗粒团状的饱满卵应为无效卵 ,不会孵化 ;颜色发亮的卵处理后胚胎外貌清晰可见 ,此种卵当天即可破壳。棉蚜卵为滞育卵 ,春季降水对孵化有促进作用 ;室外棉蚜卵的饱满率和饱满卵的孵化率较低。该地区秋冬气候特点可能是石河子地区棉蚜卵低温条件下安全越冬的重要因素     

用三维图象量测卵裂前蛙卵膜分子的三维运动

两栖类卵第一次卵裂前,缩时电影显示出卵表面有收缩波。由于卵的体积未变,在收缩时卵的高度必然增加。Sawai(1978)利用棱镜侧面摄取了蝾螈卵轮廓的高度变化,证实了卵裂前卵最高处的高度确有增加。但这一方法不能测知整个卵表面各处的高度变化,而且仅是二维的。在林蛙卵上,我们用荧光漂白恢复技术发现第一次卵裂前卵表面分子有规律性的流动,推测这是卵球的张弛。为了进一步     

桃小食心虫卵收集方法的改进

本文介绍了一种用绒面壁纸作为卵卡收集桃小食心虫Carposina sasakii Matsumura卵的方法。利用显微镜测试了绒面的绒毛高度和密度,并从落卵量和卵的孵化率两方面对这种卵卡和传统的滤纸卵卡进行了比较。结果表明,滤纸卵卡和绒面卵卡上的总落卵量无显著差异,平均为(303.77±51.03)粒和(330.23±44.85)粒,其中成虫交尾后48 h内的落卵量平均为(303.77±51.03)粒和(330.23±44.85)粒,其中成虫交尾后48 h内的落卵量为(176.31±38.96)粒和(223.92±30.69)粒(P<0.001)。成虫交尾后48 h内产下的卵平均孵化率为93.97%和94.56%,48 h后产下的卵平均孵化率为83.87%和83.58%,即成虫交尾后48 h后产下的卵的孵化率显著低于交尾后48 h内产下的卵(P<0.001),但同期落于两种卵卡上的卵孵化率差异不大。因此,使用绒面卵卡能显著提高初孵幼虫的数量,在得到相同虫量的情况下,显著降低成本。且相对于人工刮制的传统卵卡,使用绒面卵卡,很好的避免了因手工制作导致的一致性差、耗时长、人工费昂贵的问题,为收集桃小食心虫卵提供了一种较为理想的方法。     

Identification of pelagic eggs of marine fishes by rearing method

Pelagic fish eggs are usually fixed by formalin solution just after collection in the field. Most of these eggs are difficult to be identified to species, because only limited characters are available for identification and considerable changes in structures take place with fixation. In this study, species names of formalin fixed eggs were estimated by comparing their egg diameters and the diameter and number of oil globules with those of the fresh ones identified by the rearing method. Materials were collected in Wakasa Bay in May, August, and October, 1979–1982. Fresh eggs were classified into 40 species or types by the rearing method, but fixed eggs were divided into only 24 types. Comparison of fresh and fixed eggs revealed that 7 out of 24 types of fixed eggs were referable to species, and 13 types were composed of species groups. The rearing method is surely a useful step in indentifying species names and/or species types of fixed eggs.     

A saltwater flotation technique to identify unincubated eggs

ABSTRACT.   Field studies on nesting birds sometimes involve questions related to nest initiation dates, length of the incubation period, or changes in parental incubation behavior during various stages of incubation. Some of this information can be best assessed when a nest is discovered before the eggs have undergone any incubation, and this has traditionally been assessed by floating eggs in freshwater. However, because the freshwater method is not particularly accurate in identifying unincubated eggs, we developed a more reliable saltwater flotation method. The saltwater method involves diluting a saturated saltwater solution with freshwater until a salt concentration is reached where unincubated eggs sink to the bottom and incubated eggs float to the surface. For Laughing Gulls ( Leucophaeus atricilla ), floating eggs in freshwater failed to identify 39.0% ( N = 251) of eggs that were subsequently found by candling to have undergone incubation prior to collection. By contrast, in a separate collection of gull eggs, no eggs that passed the saltwater test ( N = 225) were found by a later candling to have been incubated prior to collection. For Double-crested Cormorants ( Phalacrocorax auritus ), floating eggs in freshwater failed to identify 15.6% ( N = 250) of eggs that had undergone incubation prior to collection, whereas in a separate collection, none of the eggs that passed the saltwater test ( N = 85) were found by a later candling to have been incubated prior to collection. Immersion of eggs in saltwater did not affect embryo survival. Although use of the saltwater method is likely limited to colonial species and requires calibrating a saltwater solution, it is a faster and more accurate method of identifying unincubated eggs than the traditional method of floating eggs in freshwater.     

Inactivation of viable Ascaris eggs by reagents during enumeration.

Various reagents commonly used to enumerate viable helminth eggs from wastewater and sludge were evaluated for their potential to inactivate Ascaris eggs under typical laboratory conditions. Two methods were used to enumerate indigenous Ascaris eggs from sludge samples. All steps in the methods were the same except that in method I a phase extraction step with acid-alcohol (35% ethanol in 0.1 N H(2)SO(4)) and diethyl ether was used whereas in method II the extraction step was avoided by pouring the sample through a 38-microm-mesh stainless steel sieve that retained the eggs. The concentration of eggs and their viability were lower in the samples processed by method I than in the samples processed by method II by an average of 48 and 70%, respectively. A second set of experiments was performed using pure solutions of Ascaris suum eggs to elucidate the effect of the individual reagents and relevant combination of reagents on the eggs. The percentages of viable eggs in samples treated with acid-alcohol alone and in combination with diethyl ether or ethyl acetate were 52, 27, and 4%, respectively, whereas in the rest of the samples the viability was about 80%. Neither the acid nor the diethyl ether alone caused any decrease in egg viability. Thus, the observed inactivation was attributed primarily to the 35% ethanol content of the acid-alcohol solution. Inactivation of the eggs was prevented by limiting the direct exposure to the extraction reagents to 30 min and diluting the residual concentration of acid-alcohol in the sample by a factor of 100 before incubation. Also, the viability of the eggs was maintained if the acid-alcohol solution was replaced with an acetoacetic buffer. None of the reagents used for the flotation step of the sample cleaning procedure (ZnSO(4), MgSO(4), and NaCl) or during incubation (0.1 N H(2)SO(4) and 0.5% formalin) inactivated the Ascaris eggs under the conditions studied.     

Treatment of Salmonella-Arizona-Infected Turtle Eggs with Terramycin and Chloromycetin by the Temperature Differential Egg Dip Method

Attempts to eliminate Salmonella and Arizona infection from newly hatched turtles were made by dipping fresh eggs in cold solutions of Terramycin and Chloromycetin at 1,000, 1,200, 1,500 and 2,000 mug per ml for either 10, 20, or 30 min. Control groups consisted of hatchings produced from nondipped eggs or eggs dipped in chilled water. In two of the four experiments 5 to 10 eggs were blended on days 15, 30, and 45 post antibiotic dip treatment. Twenty-five to 60 hatchlings from each control or experimental dip groups were held in containers and the water was tested (excretion method) for Salmonella and Arizona every 15 or 30 days for 180 to 210 days after hatching. Representative turtles were homogenized (blending method) to determine if systemic infections were present. All specimens tested were enriched in tetrathionate and selenite cystine broth. Nondipped eggs and water-dipped eggs routinely showed Salmonella and Arizona present in egg homogenate and hatchlings emerging from these eggs excreted these pathogens. Terramycin- and Chloromycetin-dipped eggs were uniformly negative for these pathogens, only if fresh eggs were dipped. Bacteriological assay of container water and whole turtle homogenate from hatchlings were negative for Salmonella and Arizona if eggs were dipped in 1,000 mug of Terramycin early in the egg laying season or if eggs were dipped in 1,500 or 2,000 mug of Terramycin per ml late in the egg laying season. The results of temperature-differential egg dip studies suggest that this is a feasible and promising method by which to eradicate Salmonella and Arizona from the turtle.     

Modified sugar centrifugal flotation technique for recovering Echinococcus multilocularis eggs from soil

Among soil-transmitted parasitic diseases, alveolar hydatidosis due to the ingestion of Echinococcus multilocularis eggs is becoming a serious problem in Hokkaido, the northern most island of Japan. Dissemination of the infection far from the endemic areas can occur if motor vehicles transmit soil contaminated with eggs. No appropriate and validated method for recovering the taeniid eggs from soil is available. A modified sugar centrifugal flotation technique, using a sucrose solution of specific gravity 1.27 and 0.05% Tween-80, was evaluated as a method to successfully recover eggs from soil. Contamination levels as low as 10 eggs per gram could be detected. This method may be useful to determine the prevalence of E. multilocularis, its transmission, and the potential for by monitoring soil contamination with eggs.     

一种改进的显微注射用DNA片段的纯化方法

目的显微注射用DNA的纯度是影响转基因动物制备成功与否的重要因素,本文建立一种可行的适用于普通实验室的纯化DNA方法,替代普遍使用的试剂盒纯化方法。方法分别使用酚-氯仿多次抽提法及常规的凝胶提取试剂盒纯化含有蚓激酶基因的DNA片段,通过显微注射技术将纯化的DNA片段导入小鼠受精卵的原核,制备转基因小鼠。根据转基因实验的结果对两种方法进行比较。结果使用两种方法纯化DNA均能获得转基因小鼠。在DNA纯度及注射卵的存活率上,两种方法无明显差别;在移植卵的出生率及转基因阳性率上,抽提法优于试剂盒法。结论本实验建立的抽提方法可以替代试剂盒方法纯化显微注射用DNA片段,在降低实验成本、简化实验条件及提高转基因阳性率方面具有优势。     

黏性卵鱼类受精卵一种快速高效的显微注射方法

黏性卵鱼类受精卵遇水后产生的黏性和卵壳变硬的现象严重影响着大批量显微注射操作的速度和随后的取材。研究建立了一种高效的黏性受精卵快速脱黏显微注射方法, 并利用荧光标记葡聚糖Alex-Fluor488-dextran评估了消化脱黏、直接注射和脱壳注射三种方法的技术特点和适用范围。结果表明: 在23℃, 用0.25%胰蛋白酶(pH=7.1-7.4)消化4min可获得脱黏受精卵。与直接注射和脱壳注射方法相比, 研究建立的消化脱黏方法兼具二者的优点: 在受精后5min可以开始显微操作, 无黏性, 容易进针, 胚盘清晰便于观察、注射后容易培养和取材。实验方法适用于研究与黏性卵鱼类卵子发生、卵-胚转换和早期胚胎发育密切相关基因的功能, 亦可满足追踪受精过程中核质细微变化研究的需要。     

杨扇舟蛾卵和幼虫的空间分布型及抽样技术

研究了杨扇舟蛾Clostera anachoreta(Fabricius)卵和幼虫的空间分布型及抽样技术,结果表明杨扇舟蛾卵和幼虫在杨树林的分布型均为聚集型中的负二项分布。几种抽样方法中,卵以棋盘式最好,幼虫以平行线法最好。同时建立了杨扇舟蛾卵的下层抽样模型为y=2.4481x 0.4243;幼虫的中、下层抽样模型为y=2.4605x 3.9126。     

Simultaneous measurement of fluoroquinolones in eggs by a combination of supercritical fluid extraction and high pressure liquid chromatography

Simultaneous detection of the fluoroquinolone antibiotics ciprofloxacin, enrofloxacin, ofloxacin, and norfloxacin in eggs by a combination of supercritical fluid extraction (SFE) and high pressure liquid chromatography (HPLC) was studied. Lipid matrices that have been considered to result in poor extraction and isolation of fluoroquinolones in eggs were removed first by SFE with supercritical CO(2) alone, and then the fluoroquinolones were extracted by SFE with supercritical CO(2) containing 20% (v/v) methanol for HPLC analysis. A time-course study of the extraction of lipid matrices of eggs suggested that the SFE method successfully removed the matrices within 20 min. When the fluoroquinolones added to control eggs were extracted by SFE, the extraction efficiency was similar to that by the solvent extraction method, giving the recovery percentages from 83 to 96% in a 40 min-extraction time. The fluoroquinolones extracted from eggs by SFE were analyzed simultaneously by HPLC equipped with a fluorescence detector with detection sensitivity at about 10 ppb for the detection limit. The standard calibration profiles of fluoroquinolones showed linear responses to HPLC, showing more than 0.995 for the mean r(2) value. This is the first report of the simultaneous measurement of fluoroquinolones in eggs by a combination of SFE and HPLC. Using the SFE method allowed us to avoid extensive sample preparation such as solvent extraction and chromatographic cleanup that are basically required in extraction of fluoroquinolones.     

The effect of the nucleocytoplasmic ratio on protein synthesis and expression of a stage-specific antigen in early cleaving mouse embryos

The nucleocytoplasmic ratio of fertilized mouse eggs was manipulated by removing or injecting cytoplasm by micropipette, and bisection of denuded eggs to obtain both pronuclei in one half of the eggs cytoplasm. The experimental eggs were capable of cleavage to the morula stage and, in some instances, developed to the blastocyst stage similar to unmanipulated eggs. The removal of large quantities of cytoplasm by micropipette and injecting them into a recipient egg did not provide sufficient numbers of viable eggs, whereas transfer of smaller quantities (about a quarter of the cytoplasm) was less deleterious, at least for recipient eggs. However, the alteration of the nucleocytoplasmic ratio by this method was not of the correct magnitude for the purpose of this experiment. Therefore, bisection was the preferred method whereby the nucleocytoplasmic ratio was doubled. This resulted in both pronuclei residing in one half of the egg's cytoplasm. Half eggs with one pronucleus (haploid) but retaining a nucleocytoplasmic ratio similar to unmanipulated control eggs served as additional controls for the bisection experiments. Protein synthesis was analysed by two-dimensional gel electrophoresis, showing that the 2-cell- and 4-cell-stage bisected embryos with double and normal nucleocytoplasmic ratio expressed equivalent protein synthesis patterns as control embryos of the same stage. Likewise, the stage-specific surface antigen SSEA-1 did not appear before the 6- to 8-cell stage. Also in cytoplasm transfer experiments, there was no indication that altering the nucleocytoplasmic ratio in either direction changed the timing of stage-specific gene expression. These results support the idea that stage-specific gene activity during early mouse cleavage might proceed in parallel to DNA replication cycles and is independent of the nucleocytoplasmic ratio.