33 Boron in diatoms

Lewin, J. C. (1965) showed that boron is required for the growth of Cylindrotheca fusiformis , and, presumably, other diatoms too. It may be involved in cellular metabolism, as in higher plants, or incorporated by accident or design into the siliceous skeletons (frustules), since B 2 O 3 has been pr...

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Published in:Journal of Phycology
Main Authors: Deyhle, A., Hodge, V., Lewin, R. A.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2003
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Online Access:http://dx.doi.org/10.1111/j.0022-3646.2003.03906001_33.x
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spelling crwiley:10.1111/j.0022-3646.2003.03906001_33.x 2024-06-02T08:09:25+00:00 33 Boron in diatoms Deyhle, A. Hodge, V. Lewin, R. A. 2003 http://dx.doi.org/10.1111/j.0022-3646.2003.03906001_33.x https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.0022-3646.2003.03906001_33.x https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.0022-3646.2003.03906001_33.x en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Phycology volume 39, issue s1, page 12-13 ISSN 0022-3646 1529-8817 journal-article 2003 crwiley https://doi.org/10.1111/j.0022-3646.2003.03906001_33.x 2024-05-03T11:06:00Z Lewin, J. C. (1965) showed that boron is required for the growth of Cylindrotheca fusiformis , and, presumably, other diatoms too. It may be involved in cellular metabolism, as in higher plants, or incorporated by accident or design into the siliceous skeletons (frustules), since B 2 O 3 has been proven to replace SiO 2 (e.g. in siliceous rocks). Thus the frustules may contain or bear at their surface a proportion of borosilica, which might reduce their solubility in water. (Incidentally, boron has also been implicated in human bone formation and stability (Newnham, 1994). Deyhle (2002), who determined the content of B in calcareous skeletons of marine foraminifera and compared the isotopic ratios of 11 B /10 B with that in the environmental sea water, found the B content to be generally less than 10 ppm We sought comparable values for diatom frustules, washed and bleached to remove salts and organic matter, if possible without leaching away any of the B that could be present. We studied fossil diatomite from Lompoc, California; diatomaceous ooze from Myvatn, Iceland; natural plankton diatoms harvested from the sea; and pure cultures of marine and freshwater diatoms grown in the laboratory. By contrast with foraminiferan calcite, our data indicated that diatom frustules contain up to 1,600 ppm of boron, with a more marked enrichment of the lighter isotope. Rough calculations indicate that the B 2 O 3 , even if concentrated at the frustule surface, might be enough to reduce the solubility of the frustules. Our B‐isotope enrichment data range between +3.9 to −0.2‰, indicating that diatoms preferentially incorporate the light 10 B . Such values can provide indications to physico‐chemical conditions under which the skeletons were deposited (cf. Lewin, E. et al. 2000) Data will be presented. Article in Journal/Newspaper Iceland Wiley Online Library Journal of Phycology 39 s1 12 13
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description Lewin, J. C. (1965) showed that boron is required for the growth of Cylindrotheca fusiformis , and, presumably, other diatoms too. It may be involved in cellular metabolism, as in higher plants, or incorporated by accident or design into the siliceous skeletons (frustules), since B 2 O 3 has been proven to replace SiO 2 (e.g. in siliceous rocks). Thus the frustules may contain or bear at their surface a proportion of borosilica, which might reduce their solubility in water. (Incidentally, boron has also been implicated in human bone formation and stability (Newnham, 1994). Deyhle (2002), who determined the content of B in calcareous skeletons of marine foraminifera and compared the isotopic ratios of 11 B /10 B with that in the environmental sea water, found the B content to be generally less than 10 ppm We sought comparable values for diatom frustules, washed and bleached to remove salts and organic matter, if possible without leaching away any of the B that could be present. We studied fossil diatomite from Lompoc, California; diatomaceous ooze from Myvatn, Iceland; natural plankton diatoms harvested from the sea; and pure cultures of marine and freshwater diatoms grown in the laboratory. By contrast with foraminiferan calcite, our data indicated that diatom frustules contain up to 1,600 ppm of boron, with a more marked enrichment of the lighter isotope. Rough calculations indicate that the B 2 O 3 , even if concentrated at the frustule surface, might be enough to reduce the solubility of the frustules. Our B‐isotope enrichment data range between +3.9 to −0.2‰, indicating that diatoms preferentially incorporate the light 10 B . Such values can provide indications to physico‐chemical conditions under which the skeletons were deposited (cf. Lewin, E. et al. 2000) Data will be presented.
format Article in Journal/Newspaper
author Deyhle, A.
Hodge, V.
Lewin, R. A.
spellingShingle Deyhle, A.
Hodge, V.
Lewin, R. A.
33 Boron in diatoms
author_facet Deyhle, A.
Hodge, V.
Lewin, R. A.
author_sort Deyhle, A.
title 33 Boron in diatoms
title_short 33 Boron in diatoms
title_full 33 Boron in diatoms
title_fullStr 33 Boron in diatoms
title_full_unstemmed 33 Boron in diatoms
title_sort 33 boron in diatoms
publisher Wiley
publishDate 2003
url http://dx.doi.org/10.1111/j.0022-3646.2003.03906001_33.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.0022-3646.2003.03906001_33.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.0022-3646.2003.03906001_33.x
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op_source Journal of Phycology
volume 39, issue s1, page 12-13
ISSN 0022-3646 1529-8817
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