Dynamics of formation and secretion of heterococcoliths by Coccolithus pelagicus ssp. braarudii

• Published in: European journal of phycology Vol. 42; no. 2; pp. 125 - 136
• Main Authors: Taylor, Alison R., Russell, Mark A., Harper, Glenn M., Collins, Toby f. T., Brownlee, Colin
• Format: Journal Article
• Language: English
• Published: Taylor & Francis Group 01-05-2007
• Subjects: calcification; coccolithophore; Coccolithus huxleyi; Coccolithus pelagicus; cytoskeleton; Emiliania huxleyi; endoplasmic reticulum; exocytosis; Golgi body; Marine; photosynthesis; secretion
• ISSN: 0967-0262; 1469-4433
• DOI: 10.1080/09670260601159346

The formation and secretion of heterococcoliths by the non-motile life phase of the coccolithophore Coccolithus pelagicus was investigated using electron microscopy and time-lapse bright field imaging. Coccolithogenesis in C. pelagicus exhibited sequential mineralization of single coccoliths in Golgi-derived and nuclear-associated vesicles, a pattern similar to the formation of heterococcoliths in Emiliania huxleyi. Our TEM data show that only on maturation does the single coccolith vesicle migrate away from the nucleus before secretion. A reticular body, distinct from the Golgi body, was also clearly visible at the distal surface of the developing coccolith vesicle, suggesting this is a common structural feature in placolith cells that mineralize and secrete coccoliths one at a time. Time-lapse imaging revealed that the coccolith secretion process is rapid, taking 60-190 seconds, and involves considerable contractile activity to eject and position the coccolith on the surface of the cell. An intact flagellar root apparatus was discovered at the anterior pole of this non-motile cell from which polarized secretion of coccoliths occurs, which may indicate a novel role for such cytoskeletal structures. Freeze-fracture preparations revealed columnar deposits and adhesions linking the scales and coccolith baseplates to the cell, across the periplasmic space providing points of attachment for cellular movement. Rotatory movements of the cell relative to external coccoliths were exhibited by all actively calcifying cells. These movements enable the cell, while exhibiting morphologically polarized secretion, to locate and secrete a mature coccolith in a spatially well-defined manner. Finally, the time-lapse imaging approach described here provides an opportunity to quantify the regulation of coccolith production in single cells with high temporal resolution allowing responses of calcification to rapidly fluctuating environmental conditions such as light-dark transitions to be examined in detail, which has not been possible with bulk calcification studies.