Nordengen I, Klingen I
Bioforsk, Norwegian Institute for Agricultural and Environmental Research, Department of Entomology and Nematology, Norway.
J Invertebr Pathol. 2006 May;92(1):1-6. doi: 10.1016/j.jip.2006.01.005. Epub 2006 Mar 13.
Methods for measuring prevalence of Neozygites floridana in a Tetranychus urticae population collected from strawberries were developed and compared. T. urticae were extracted from leaves using a soapy water solution (0.5 ml washing detergent : 8 L water) and then placed into 80% alcohol for use in Methods 1 and 2. Method 1: N. floridana-sporulating T. urticae cadavers were observed and quantified under a compound microscope (40-80x). Method 2: Adult females were mounted in lactophenol cotton blue and observed for the presence or absence of N. floridana hyphal bodies under a microscope (200-400x). Method 3: Live T. urticae females were incubated at 25 degrees C and 75% RH and observed for mortality and N. floridana infection under a compound microscope (6.4-40x). Method 1 was the most time-efficient method and it also allows processing of samples as time permits. Method 2 quantified significantly higher fungal prevalence than Methods 1 and 3, but Method 2 is not considered to be reliable because hyphal bodies are difficult to detect. No significant differences were found between Methods 1 and 3.
我们开发并比较了从草莓上采集的二斑叶螨种群中弗罗里达新接霉(Neozygites floridana)患病率的测量方法。使用肥皂水溶液(0.5毫升洗涤液:8升水)从叶片中提取二斑叶螨,然后将其放入80%的酒精中,用于方法1和方法2。方法1:在复式显微镜(40 - 80倍)下观察并量化带有弗罗里达新接霉孢子的二斑叶螨尸体。方法2:将成年雌螨固定在乳酸酚棉蓝中,在显微镜(200 - 400倍)下观察是否存在弗罗里达新接霉的菌丝体。方法3:将活的二斑叶螨雌螨在25摄氏度和75%相对湿度下培养,在复式显微镜(6.4 - 40倍)下观察死亡率和弗罗里达新接霉感染情况。方法1是最省时的方法,并且也允许在时间允许的情况下处理样本。方法2量化的真菌患病率显著高于方法1和方法3,但方法2不被认为可靠,因为菌丝体难以检测。方法1和方法3之间未发现显著差异。