Gavaia P J, Sarasquete C, Cancela M L
Center for Marine Sciences, University of Algarve, Faro, Portugal.
Biotech Histochem. 2000 Mar;75(2):79-84. doi: 10.3109/10520290009064151.
We have developed a procedure for staining cartilage and bone in fish larvae as small as 2 mm (notochord length), for which standard alcian blue/alizarin red procedures did not give positive and/or consistent results. Small calcified structures only 100-200 microns in length can be clearly visualized. The method is suitable for both ontogenic studies during early stages of skeletal development in most marine fishes (e.g., Sparus aurata L., Solea senegalensis Kaup), whose larvae at hatching are often only a few millimeters long and for detecting skeletal abnormalities in small larvae. This procedure can also be used for specimens that have been preserved in 100% ethanol for up to two years.
我们开发了一种对体长仅2毫米(脊索长度)的鱼类幼虫的软骨和骨骼进行染色的方法,而标准的阿尔新蓝/茜素红方法并未给出阳性和/或一致的结果。仅100 - 200微米长的小钙化结构能够清晰可见。该方法适用于大多数海洋鱼类骨骼发育早期阶段的个体发育研究(例如,金头鲷、塞内加尔鳎),这些鱼类的幼虫在孵化时通常只有几毫米长,也适用于检测小幼虫的骨骼异常。此方法还可用于保存在100%乙醇中长达两年的标本。