Diurnal and bathymetric changes in chlorophyll fluorescence yields of reef corals measured in situ with a fast repetition rate fluorometer

A newly developed underwater fast repetition rate fluorometer (FRRF) was used for in situ measurements of chlorophyll fluorescence yields on the reef-building corals Montastraea faveo- lata and Montastraea cavernosa from around Lee Stocking Island, Bahamas. Diel studies of the quan- tum yield of chlorophyll fluorescence (⌉F '/ Fm') in photosystem II (PSII) reveal a pattern of mid-day depression of ⌉F '/ Fm' in both of these species of coral. At the same time, non-photochemical quench- ing (qN ) increased significantly during the day, a pattern consistent with the regulation of PSII by dynamic photoinhibition mediated by non-photochemical quenching. Despite these mid-day depres- sions in ⌉F '/ Fm', net productivity, measured as oxygen flux, remains high, suggesting that non-pho- tochemical quenching dissipates the majority of the absorbed photons at mid-day and protects the photosynthetic apparatus, allowing the endosymbiotic dinoflagellates (zooxanthellae) to operate at maximum rates of photosynthesis. In 1999 measurements of ⌉F '/ Fm' on M. faveolata over a bathy- metric range of 2 to 30 m showed an increase in ⌉F '/ Fm' with increasing depth when measured at the same time of day. This suggests, although there is year-to-year variability, that changes in the under- water light field, and photoacclimation to that light field, control the degree of photoprotection attrib- utable to non-photochemical quenching in the zooxanthellae of these corals. The fluorescence yields of M. faveolata exposed to elevated temperatures (> 32°C) in the field showed a significant decrease in ⌉F '/Fm' before visible signs (e.g., paling of colonies) occurred. It was also possible to predict which colonies at the same depth and light regime would bleach first in response to elevated temperatures before any visible signs of bleaching were evident using ⌉F '/Fm' as a predictor.

[1]  Zbigniew S. Kolber,et al.  Variations in Chlorophyll Fluorescence Yields in Phytoplankton in the World Oceans , 1995 .

[2]  P. Falkowski,et al.  POPULATION CONTROL IN SYMBIOTIC CORALS , 1993 .

[3]  G. Samson,et al.  Origins of the low yield of chlorophyll a fluorescence induced by single turnover flash in spinach thylakoids , 1996 .

[4]  P. Falkowski,et al.  Photosynthesis and photoprotection in symbiotic corals , 2001 .

[5]  K. Asada,et al.  Production and scavenging of active oxygen in photosynthesis , 1987 .

[6]  M. Lesser Elevated temperatures and ultraviolet radiation cause oxidative stress and inhibit photosynthesis in ymbiotic dinoflagellates , 1996 .

[7]  G. Krause,et al.  Chlorophyll Fluorescence and Photosynthesis: The Basics , 1991 .

[8]  W. Fitt,et al.  Diurnal changes in photochemical efficiency and xanthophyll concentrations in shallow water reef corals : evidence for photoinhibition and photoprotection , 1999, Coral Reefs.

[9]  P. Falkowski,et al.  Measurements of variable chlorophyll fluorescence using fast repetition rate techniques: defining methodology and experimental protocols , 1998, Biochimica et biophysica acta.

[10]  W. Vincent MECHANISMS OF RAPID PHOTOSYNTHETIC ADAPTATION IN NATURAL PHYTOPLANKTON COMMUNITIES. II. CHANGES IN PHOTOCHEMICAL CAPACITY AS MEASURED BY DCMU‐INDUCED CHLOROPHYLL FLUORESCENCE 1 , 1980 .

[11]  J. Marsh,et al.  Primary productivity of reef-building calcareous red algae , 1970 .

[12]  P. Falkowski,et al.  Measurement of photosynthetic parameters in benthic organisms in situ using a SCUBA‐based fast repetition rate fluorometer , 2000 .

[13]  O. Hoegh‐Guldberg,et al.  Photoinhibition and photoprotection in symbiotic dinoflagellates from reef-building corals , 1999 .

[14]  B. Osborne,et al.  Light and Photosynthesis in Aquatic Ecosystems. , 1985 .

[15]  G. Schmidt,et al.  Damage to photosystem II in symbiotic dinoflagellates: a determinant of coral bleaching. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[16]  O. Hoegh‐Guldberg,et al.  Temperature‐induced bleaching of corals begins with impairment of the CO2 fixation mechanism in zooxanthellae , 1998 .

[17]  P. Ralph,et al.  In situ underwater measurements of photosynthetic activity of coral zooxanthellae and other reef-dwelling dinoflagellate endosymbionts , 1999 .

[18]  B. Demmig‐Adams,et al.  The role of xanthophyll cycle carotenoids in the protection of photosynthesis , 1996 .

[19]  R. Iglesias-Prieto,et al.  Photosynthetic response to elevated temperature in the symbiotic dinoflagellate Symbiodinium microadriaticum in culture. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[20]  I. Ohad,et al.  Membrane protein damage and repair: Selective loss of a quinone-protein function in chloroplast membranes. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Mark E. Warner,et al.  The effects of elevated temperature on the photosynthetic efficiency of zooxanthellae in hospite from four different species of reef coral: a novel approach , 1996 .

[22]  P. Falkowski,et al.  Effects of Growth Irradiance and Nitrogen Limitation on Photosynthetic Energy Conversion in Photosystem II. , 1988, Plant physiology.

[23]  Mark W. Denny,et al.  Pulsed delivery of subthermocline water to Conch Reef (Florida Keys) by internal tidal bores , 1996 .

[24]  W. L. Butler On the primary nature of fluorescence yield changes associated with photosynthesis. , 1972, Proceedings of the National Academy of Sciences of the United States of America.