Phytoplankton photosynthetic parameters in waters near the Kamchatka Peninsula in August–September 2023
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Abstract
The climate change and increasing anthropogenic load affect the aquatic ecosystems. State and productivity of pelagic ecosystems are largely determined by photosynthetic capacity of phytoplankton. The aim of this work was to analyze the variability of phytoplankton photosynthetic parameters [quantum yield of photosynthesis (ϕ) which characterizes efficiency of absorbed light quanta utility in photosynthesis, its potential capacity (ϕmax), and light-saturation coefficient (Ik)] depending on light conditions, which are determined by the ratio of thickness of the upper mixed layer (UML) to the depth of the euphotic zone (Zeu). The study covered data obtained in the Pacific Ocean and the Sea of Okhotsk during the cruise 23/4 of the RV “Professor Multanovskiy” in August–September 2023. Parameters ϕmax and Ik were calculated based on measurements of rapid light–response curves of variable fluorescence. As found out, variability in photosynthetic parameters was mainly determined by phytoplankton physiological acclimation to light. Importantly, acclimation to light, which differed between the UML and the deeper layer of the Zeu, resulted in distinct light–response patterns of relative electron transport rate curves. The values of Ik were directly related to light intensity. Nonetheless, the values of ϕmax were inversely related to light intensity, but to a larger extent than the values of Ik. As a result, ϕ, which depends on Ik and ϕmax, dropped with increasing light intensity. A tight relationship between the values of ϕ and light intensity (r = 0.97) was revealed (p < 0.0001), and it was described by an exponential function. This analysis showed peculiarities of the light forcing variability in photosynthetic parameters. The revealed dependences of Ik, ϕmax, and ϕ on light intensity can be used for express assessment of their values based on light; this is necessary for analysis of primary production involving spectral approach.
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References
Antal T., Konyukhov I., Volgusheva A., Plyusnina T., Khruschev S., Kukarskikh G., Rubin A. Chlorophyll fluorescence induction and relaxation system for the continuous monitoring of photosynthetic capacity in photobioreactors. Physiologia Plantarum, 2019, vol. 165, no. 3, pp. 476–486. https://doi.org/10.1111/ppl.12693
Babin M. Phytoplankton fluorescence: Theory, current literature and in situ measurement. In: Real-time Coastal Observing Systems for Marine Ecosystem Dynamics and Harmful Algal Blooms: Theory, Instrumentation and Modelling / M. Babin, C. S. Roesler, J. J. Cullen (Eds). Paris : UNESCO Publishing, 2008, pp. 237–280.
Babin M., Morel A., Claustre H., Bricaud A., Kolber Z., Falkowski P. G. Nitrogen- and irradiance-dependent variations of the maximum quantum yield of carbon fixation in eutrophic, mesotrophic and oligotrophic marine systems. Deep Sea Research Part I: Oceanographic Research Papers, 1996, vol. 43, iss. 8, pp. 1241–1272. https://doi.org/10.1016/0967-0637(96)00058-1
Baker N. R. Photoinhibition of photosynthesis. In: Light as an Energy Source and Information Carrier in Plant Physiology / R. C. Jennings, G. Zucchelli, F. Ghetti, G. Colombetti (Eds). Boston, MA : Springer US, 1996, pp. 89–97. https://doi.org/10.1007/978-1-4613-0409-8
Bannister T. T. Quantitative description of steady state, nutrient-saturated algal growth, including adaptation. Limnology and Oceanography, 1979, vol. 24, iss. 1, pp. 76–96. https://doi.org/10.4319/lo.1979.24.1.0076
Beardall J., Young E., Roberts S. Approaches for determining phytoplankton nutrient limitation. Aquatic Sciences, 2001, vol. 63, iss. 1, pp. 44–69. https://doi.org/10.1007/pl00001344
Behrenfeld M. J., Kolber Z. S. Widespread iron limitation of phytoplankton in the south Pacific Ocean. Science, 1999, vol. 283, no. 5403, pp. 840–843. https://doi.org/10.1126/science.283.5403.840
Behrenfeld M. J., Prasil O., Babin M., Bruyant F. In search of a physiological basis for covariations in light-limited and light-saturated photosynthesis. Journal of Phycology, 2004, vol. 40, iss. 1, pp. 4–25. https://doi.org/10.1046/j.1529-8817.2004.03083.x
Björkman O., Demmig B. Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins. Planta, 1987, vol. 170, iss. 4, pp. 489–504. https://doi.org/10.1007/bf00402983
Brainerd K. E., Gregg M. C. Surface mixed and mixing layer depths. Deep Sea Research Part I: Oceanographic Research Papers, 1995, vol. 42, iss. 9, pp. 1521–1543. https://doi.org/10.1016/0967-0637(95)00068-h
Bricaud A., Roesler C. S., Parslow J. S., Ishizaka J. Bio-optical studies during the JGOFS-equatorial Pacific program: A contribution to the knowledge of the equatorial system. Deep Sea Research Part II: Topical Studies in Oceanography, 2002, vol. 49, iss. 13–14, pp. 2583–2599. https://doi.org/10.1016/s0967-0645(02)00049-8
Chow W. S, Aro E.-M. Photoinactivation and mechanisms of recovery. In: Photosystem II. The Light-Driven Water: Plastoquinone Oxidoreductase / T. Wydrzynski, K. Satoh (Eds). Netherlands : Springer, 2005, pp. 627–648. https://doi.org/10.1007/1-4020-4254-x
Churilova T., Suslin V., Krivenko O., Efimova T., Moiseeva N. Spectral approach to assessment of phytoplankton photosynthesis rate in the Black Sea based on satellite information methodological aspects of the regional model development. Journal of Siberian Federal University. Biology, 2016, vol. 9, iss. 4, pp. 367–384. (in Russ.). https://doi.org/10.17516/1997-1389-2016-9-4-367-384
Cota G. F., Smith W. O., Mitchell B. G. Photosynthesis of Phaeocystis in the Greenland Sea. Limnology and Oceanography, 1994, vol. 39, iss. 4, pp. 948–553. https://doi.org/10.4319/lo.1994.39.4.0948
Cruz S., Serôdio J. Relationship of rapid light curves of variable fluorescence to photoacclimation and non-photochemical quenching in a benthic diatom. Aquatic Botany, 2008, vol. 88, iss. 3, pp. 256–264. https://doi.org/10.1016/j.aquabot.2007.11.001
Evolution of Primary Producers in the Sea / P. Falkowski, A. H. Knoll (Eds). New York ; London ; Oxford : Academic Press, 2011, 441 p. https://doi.org/10.1016/b978-0-12-370518-1.x5000-0
Falkowski P. G., Raven J. A. Aquatic Photosynthesis. 2nd edition. New Jersey : Princeton University Press, 2007, 488 p.
Heraud P., Beardall J. Changes in chlorophyll fluorescence during exposure of Dunaliella tertiolecta to UV radiation indicate a dynamic interaction between damage and repair processes. Photosynthesis Research, 2000, vol. 63, iss. 2, pp. 123–134. https://doi.org/10.1023/a:1006319802047
IOCCG. Ocean Optics and Biogeochemistry Protocols for Satellite Ocean Colour Sensor Validation, Volume 4.0. Inherent Optical Property Measurements and Protocols: Best Practices for the Collection and Processing of Ship-Based Underway Flow-Through Optical Data / A. R. Neeley, A. Mannino (Eds). Dartmouth, NS, Canada : International Ocean-Colour Coordinating Group (IOCCG), 2019, 22 p. (IOCCG Protocol Series ; vol. 4.0). https://doi.org/10.25607/obp-664
Isada T., Iida T., Liu H., Saitoh S. I., Nishioka J., Nakatsuka T., Suzuki K. Influence of Amur River discharge on phytoplankton photophysiology in the Sea of Okhotsk during late summer. Journal of Geophysical Research: Oceans, 2013, vol. 118, iss. 4, pp. 1995–2013. https://doi.org/10.1002/jgrc.20159
Johnson Z., Bidigare R. R., Goericke R., Marra J., Trees C., Barber R. T. Photosynthetic physiology and physicochemical forcing in the Arabian Sea, 1995. Deep Sea Research Part I: Oceanographic Research Papers, 2002, vol. 49, iss. 3, pp. 415–436. https://doi.org/10.1016/s0967-0637(01)00068-1
Kirk J. T. O. Light and Photosynthesis in Aquatic Ecosystems. 3rd edition. Cambridge : Cambridge University Press, 2011, 662 p. https://doi.org/10.1017/cbo9781139168212
Kolber Z., Wyman K. D., Falkowski P. G. Natural variability in photosynthetic energy conversion efficiency: A field study in the Gulf of Maine. Limnology and Oceanography, 1990, vol. 35, iss. 1, pp. 72–79. https://doi.org/10.4319/lo.1990.35.1.0072
Lawrenz E., Silsbe G., Capuzzo E., Ylöstalo P., Forster R. M., Simis S. G., Suggett D. J. Predicting the electron requirement for carbon fixation in seas and oceans. PloS One, 2013, vol. 8, iss. 3, art. e58137 (18 p.). https://doi.org/10.1371/journal.pone.0058137
Laws E. A. Photosynthetic quotients, new production and net community production in the open ocean. Deep Sea Research Part A. Oceanographic Research Papers, 1991, vol. 38, iss. 1, pp. 143–167. https://doi.org/10.1016/0198-0149(91)90059-o
Lee Z., Weidemann A., Kindle J., Arnone R., Carder K. L., Davis C. Euphotic zone depth: Its derivation and implication to ocean-color remote sensing. Journal of Geophysical Research: Oceans, 2007, vol. 112, no. C3, art. C03009 (11 p.). https://doi.org/10.1029/2006jc003802
Lindley S. T., Bidigare R. R., Barber R. T. Phytoplankton photosynthesis parameters along 140°W in the equatorial Pacific. Deep Sea Research Part II: Topical Studies in Oceanography, 1995, vol. 42, iss. 2–3, pp. 441–463. https://doi.org/10.1016/0967-0645(95)00029-p
MacIntyre H. L., Kana T. M., Anning T., Geider R. J. Photoacclimation of photosynthesis irradiance response curves and photosynthetic pigments in microalgae and cyanobacteria. Journal of Phycology, 2002, vol. 38, iss. 1, pp. 17–38. https://doi.org/10.1046/j.1529-8817.2002.00094.x
Marra J., Trees C. C., Bidigare R. R., Barber R. T. Pigment absorption and quantum yields in the Arabian Sea. Deep Sea Research Part II: Topical Studies in Oceanography, 2000, vol. 47, iss. 7–8, pp. 1279–1299. https://doi.org/10.1016/s0967-0645(99)00144-7
Morel A., Antoine D., Babin M., Dandonneau Y. Measured and modeled primary production in the northeast Atlantic (EUMELI JGOFS program): The impact of natural variations in photosynthetic parameters on model predictive skill. Deep Sea Research Part I: Oceanographic Research Papers, 1996, vol. 43, iss. 8, pp. 1273–1304. https://doi.org/10.1016/0967-0637(96)00059-3
Perkins R. G., Mouget J.-L., Lefebvre S., Lavaud J. Light response curve methodology and possible implications in the application of chlorophyll fluorescence to benthic diatoms. Marine Biology, 2006, vol. 149, iss. 4, pp. 703–712. https://doi.org/10.1007/s00227-005-0222-z
Platt T., Gallegos C. L., Harrison W. G. Photoinhibition of photosynthesis in natural assemblages of marine phytoplankton. Journal of Marine Research, 1980, vol. 38, pp. 687–701.
Platt T., Jassby A. D. The relationship between photosynthesis and light for natural assemblages of coastal marine phytoplankton. Journal of Phycology, 1976, vol. 12, iss. 4, pp. 421–430. https://doi.org/10.1111/j.1529-8817.1976.tb02866.x
Schreiber U. Pulse-amplitude-modulation (PAM) fluorometry and saturation pulse method: An overview. In: Chlorophyll a Fluorescence. A Signature of Photosynthesis / G. C. Papageorgiou, Govindjee (Eds). Dordrecht, the Netherlands : Springer, 2004, pp. 279–319. https://doi.org/10.1007/978-1-4020-3218-9
Schreiber U., Bilger W., Neubauer C. Chlorophyll fluorescence as a nonintrusive indicator for rapid assessment of in vivo photosynthesis. In: Ecophysiology of Photosynthesis / E.-D. Schulze, M. M. Caldwell (Eds). Berlin : Springer, 1994, pp. 49–70. https://doi.org/10.1007/978-3-642-79354-7
Schreiber U., Gademann R., Ralph P. J., Larkum A. W. D. Assessment of photosynthetic performance of Prochloron in Lissoclinum patella in hospite by chlorophyll fluorescence measurements. Plant and Cell Physiology, 1997, vol. 38, iss. 8, pp. 945–951. https://doi.org/10.1093/oxfordjournals.pcp.a029256
Serôdio J., Vieira S., Cruz S., Coelho H. Rapid light-response curves of chlorophyll fluorescence in microalgae: Relationship to steady-state light curves and non-photochemical quenching in benthic diatom-dominated assemblages. Photosynthesis Research, 2006, vol. 90, iss. 1, pp. 29–43. https://doi.org/10.1007/s11120-006-9105-5
Smyth T. J., Tilstone G. H., Groom S. B. Integration of radiative transfer into satellite models of ocean primary production. Journal of Geophysical Research: Oceans, 2005, vol. 110, iss. C10, pp. C10014.1–C10014.11. https://doi.org/10.1029/2004jc002784
Suggett D. J., Moore C. M., Hickman A. E., Geider R. J. Interpretation of fast repetition rate (FRR) fluorescence: Signatures of phytoplankton community structure versus physiological state. Marine Ecology Progress Series, 2009, vol. 376, pp. 1–19. https://doi.org/10.3354/meps07830
Vassiliev I. R., Prasil O., Wyman K. D., Kolber Z., Hanson Jr. A. K., Prentice J. E., Falkowski P. G. Inhibition of PS II photochemistry by PAR and UV radiation in natural phytoplankton communities. Photosynthesis Research, 1994, vol. 42, iss. 1, pp. 51–64. https://doi.org/10.1007/bf00019058
Vijayan A. K., Yoshikawa T., Watanabe S., Sasaki H., Matsumoto K., Saito S.-I., Takeda S., Furuya K. Influence of non-photosynthetic pigments on light absorption and quantum yield of photosynthesis in the western equatorial Pacific and the Subarctic North Pacific. Journal of Oceanography, 2009, vol. 65, iss. 2, pp. 245–258. https://doi.org/10.1007/s10872-009-0023-y
Woźniak B., Ficek D., Ostrowska M., Majchrowski R., Dera J. Quantum yield of photosynthesis in the Baltic: A new mathematical expression for remote sensing applications. Oceanologia, 2007, vol. 49, iss. 4, pp. 527–542.
Wu H., Roy S., Alami M., Green B. R., Campbell D. A. Photosystem II photoinactivation, repair, and protection in marine centric diatoms. Plant Physiology, 2012, vol. 160, iss. 1, pp. 464–476. https://doi.org/10.1104/pp.112.203067
Zhu Y., Ishizaka J., Tripathy S. C., Wang S., Mino Y., Matsuno T., Suggett D. J. Variation of the photosynthetic electron transfer rate and electron requirement for daily net carbon fixation in Ariake Bay, Japan. Journal of Oceanography, 2016, vol. 72, iss. 5, pp. 761–776. https://doi.org/10.1007/s10872-016-0370-4
Zhu Y., Ishizaka J., Tripathy S. C., Wang S., Sukigara C., Goes J., Matsuno T., Suggett D. J. Relationship between light, community composition and the electron requirement for carbon fixation in natural phytoplankton. Marine Ecology Progress Series, 2017, vol. 580, pp. 83–100. https://doi.org/10.3354/meps12310
Zhu Y., Suggett D. J., Liu C., He J., Lin L., Le F., Ishizaka J., Goes J., Hao Q. Primary productivity dynamics in the summer Arctic Ocean confirms broad regulation of the electron requirement for carbon fixation by light-phytoplankton community interaction. Frontiers in Marine Science, 2019, vol. 6, art. 275 (17 p.). https://doi.org/10.3389/fmars.2019.00275
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