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Evidence for anoxygenic photosynthesis from the distribution of bacterio-chlorophylls in the Black Sea D. J. Repeta*, D. J. Simpson*, B. B. Jorgensen‡ & H. W. Jannasch†
*Departments of Chemistry Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543, USA
†Departments of Biology, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543, USA
‡Department of Ecology and Genetics, University of Aarhus, DK-8000 Aarhus C, Denmark
THE contribution of anoxygenic photosynthesis to carbon cycling in the Black Sea, the world's largest body of anoxic marine water, has been vigorously investigated and debated for over four decades1–6. Penetration of light into the sulphide-containing deep water may result in a zone of anaerobic primary production by photosynthetic bacteria. We report here the results of analyses of photosynthetic pigments in samples of suspended particulate matter collected from two stations in the western basin of the Black Sea. Our data demonstrate high concentrations of a bacterio-chlorophyll at the chemocline, and thus the potential for anoxygenic photosynthesis as a component of primary production in the carbon cycle of the Black Sea6. More than 95% of the pigments in the bacteriochlorophyll-maximum are accounted for by a series of aromatic carotenoids and bacteriochlorophylls-e, including a previously unreported geranyl ester of 4-i-butyl bacteriochlorophyll-e. The distribution of pigments is characteristic of the obligate phototrophs Chlorobium phaeobacteroides and C. phaeovibriodes. Total depth-integrated bacteriochlorophyll at one station exceeded total chlorophyll-a in the overlying oxygenated portion of the euphotic zone. We suggest that anoxygenic photosyn-thesis is a relatively recent phenomenon in the Black Sea initiated by shallowing of the chemocline over the past decade and develop-ment of an anoxic layer devoid of O2 and H2S (ref. 7).
References
| 1. |
Kriss, A. E. & Rukina, E. A. Dokl. Akad. Nauk. SSSR 93, 1107−1110 (1953). | PubMed | ChemPort | |
| 2. |
Sorokin, Y. I. J. Cons. Int. Explor. Mer. 29, 41−53 (1964). |
| 3. |
Dickman, M. & Artuz, I. Nature 275, 191−195 (1978). |
| 4. |
Jannasch, H. W., Trüper, H. G., and Tuttle, J. H. in The Black Sea-Geology, Chemistry and Biology (eds Degens, E. & Ross, D.) 419−425 (Mem. No. 20, Am. Assn. Petrol. Geol., Tulsa, Oklahoma, 1974). |
| 5. |
Hashwa, F. A. & Trüper, H. G., Helgioländer wiss. Meeresunters. 31, 249−253 (1978). |
| 6. |
Deuser, W. G. Deep Sea Res. 18, 995−1004 (1971). | ChemPort | |
| 7. |
Murray, J. W. et al. Nature 338, 411−413 (1989). | Article | ChemPort | |
| 8. |
Liaaen-Jensen, S. Pure appl. Chem. 57, 649−658 (1985). | ChemPort | |
| 9. |
Wright, S. and Jeffrey, S. W. Mar. Ecol. Prog. Ser. 38, 259−266 (1987). | ChemPort | |
| 10. |
Liaaen-Jensen, S. in Marine Natural Products Vol. 2 (ed. Scheuer, P. J.) 2−73 (Academic, New York, 1978). |
| 11. |
Simpson, D. J. & Smith, K. M. J. Am. chem. Soc. 110, 1753−1758 (1988). | Article | ChemPort | |
| 12. |
Caple, M. B., Chow, H. & Strouse, C. E. J. biol. Chem. 253, 6730−6737 (1978). | PubMed | ChemPort | |
| 13. |
Smith, K. M., Craig, G. W., Kehres, L. A., & Pfennig, N. J. Chrom. 281, 209−223 (1983). | Article | ChemPort | |
| 14. |
Karl, D. M. & Knauer, G. A. EOS 69, 1241 (1988). |
| 15. |
Wirsen, C. O. and Jannasch, H. W. EOS 69, 1241 (1988). |
| 16. |
Liaaen-Jensen, S. Acta chem. Scand. 19, 1025−1028 (1965). | PubMed | |
| 17. |
Pfennig, N. in The Photosynthetic Bacteria (eds Clayton, R. K. & Sistrom, W. R.) 3−18 (Plenum, New York, 1978). |
| 18. |
Brockman, H., Jr Phil. Trans. R. Soc. Ser. B 273, 277−285 (1976). |
| 19. |
Trüper, H. G. & Genovese, S. Limnol. Oceanogr. 13, 225−232 (1968). | ISI | |
| 20. |
Bergstein, T., Henis, Y., and Cavari, B. Z. Can. J. Microbiol. 25, 999−1007. | PubMed | ChemPort | |
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