1976
DOI: 10.1016/s0022-5320(76)80154-2
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Fine structure of the cerebral and pygidial ocelli in Chone ecaudata (polychaeta: sabellidae)

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Cited by 124 publications
(59 citation statements)
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“…For transmission electron microscopy specimens were then prefixed in a phosphate-buffered mixture of sucrose, picric acid, glutaraldehyde and paraformaldehyde (SPAFG; Ermak and Eakin, 1976) for 2.5 h at 48C. After rinsing in the same buffer they were postfixed in buffered 1% OsO 4 for 1 h at 48C, dehydrated through a graded ethanol series (from 30 to 100%), transferred to propylene oxide, and infiltrated by the embedding medium overnight in a 1:3 mixture of embedding medium and propylene oxide.…”
Section: Methodsmentioning
confidence: 99%
“…For transmission electron microscopy specimens were then prefixed in a phosphate-buffered mixture of sucrose, picric acid, glutaraldehyde and paraformaldehyde (SPAFG; Ermak and Eakin, 1976) for 2.5 h at 48C. After rinsing in the same buffer they were postfixed in buffered 1% OsO 4 for 1 h at 48C, dehydrated through a graded ethanol series (from 30 to 100%), transferred to propylene oxide, and infiltrated by the embedding medium overnight in a 1:3 mixture of embedding medium and propylene oxide.…”
Section: Methodsmentioning
confidence: 99%
“…For electron microscopy, specimens were fixed in a phosphatebuffered mixture of sucrose, picric acid, glutaraldehyde and paraformaldehyde (SPAFG) (Ermak and Eakin, 1976) for 2.5 h at 4°C and rinsed in phosphate buffer adjusted to the osmolarity of seawater (4°C, pH 7.2, 12% sucrose). Post-fixation occurred in 1% OsO 4 for 1 h ( phosphate buffered as above) and dehydrated in a graded ethanol series.…”
Section: Electron Microscopymentioning
confidence: 99%
“…Westheide 1967 (from intertidal areas of the Island of Sylt, North Sea) and Trilobodrilus heideri Remane, 1925 (from subtidal sediments off the Island of Helgoland, North Sea; for data of the collecting site see yon Nordheim, 1984) were investigated with TEM techniques. After relaxation in a MgC12-solution the animals were fixed at 4 °C in SPAFG (sucrose-picric-acid-formaldehyde-glutaraldehyde) in phosphate buffer (+10 % sucrose) for lh (Ermak & Eakin, 1976). Then the specimens were rinsed in phosphate buffer (+10 % sucrose; pH 7.3) for 2h, postfixed at 4 °C in phosphate-buffered osmium tetroxide for lh, dehydrated in an ethanol series, embedded in an Epon-Araldite mixture, and sectioned with a diamond knife on a Reichert Uttracut, The sections were stained with aqueous uranyl acetate and lead citratel the photographs were taken with a Zeiss EM 10,…”
Section: Introductionmentioning
confidence: 99%