Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm. / Kühl, Michael; Glud, Ronnie Nøhr; Ploug, Helle; Ramsing, Niels Birger.

In: Journal of Phycology, Vol. 32, No. 5, 1996, p. 799-812.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kühl, M, Glud, RN, Ploug, H & Ramsing, NB 1996, 'Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm', Journal of Phycology, vol. 32, no. 5, pp. 799-812. https://doi.org/10.1111/j.0022-3646.1996.00799.x

APA

Kühl, M., Glud, R. N., Ploug, H., & Ramsing, N. B. (1996). Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm. Journal of Phycology, 32(5), 799-812. https://doi.org/10.1111/j.0022-3646.1996.00799.x

Vancouver

Kühl M, Glud RN, Ploug H, Ramsing NB. Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm. Journal of Phycology. 1996;32(5):799-812. https://doi.org/10.1111/j.0022-3646.1996.00799.x

Author

Kühl, Michael ; Glud, Ronnie Nøhr ; Ploug, Helle ; Ramsing, Niels Birger. / Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm. In: Journal of Phycology. 1996 ; Vol. 32, No. 5. pp. 799-812.

Bibtex

@article{d169463b22804986a1928cf22efd0f4f,
title = "Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm",
abstract = "The photosynthetic performance of an epilithic cyanobacterial biofilm was studied in relation to the in situ light field by the use of combined microsensor measurements of O2, photosynthesis, and spectral scalar irradiance. The high density of the dominant filamentous cyanobacteria (Oscillatoria sp.) embedded in a matrix of exopolymers and bacteria resulted in a photic zone of <0.7 mm. At the biofilm surface, the prevailing irradiance and spectral composition were significantly different from the incident light. Multiple scattering led to an intensity maximum for photic light (400-700 nm) of ca. 120% of incident quantum irradiance at the biofilm surface. At the bottom of the euphotic zone in the biofilm, light was attenuated strongly to <5-10% of the incident surface irradiance. Strong spectral signals from chlorophyll a (440 and 675 nm) and phycobilins (phycoerythrin 540-570 nm, phycocyanin 615-625 nm) were observed as distinct maxima in the scalar irradiance attenuation spectra in the upper 0.0-0.5 mm of the biofilm. The action spectrum for photosynthesis in the cyanobacterial layer revealed peak photosynthetic activity at absorption wavelengths of phycobilins, whereas only low photosynthesis rates were induced by light absorption of carotenoids (450-550 nm). Respiration rates in light- and dark-incubated biofilms were determined using simple flux calculations on measured O2 concentration profiles and photosynthetic rates. A significantly higher a real O2 consumption was found in illuminated biofilms than in dark-incubated biofilms. Although photorespiration accounted for part of the increase, the enhanced areal O2 consumption of illuminated biofilms could also be ascribed to a deeper oxygen penetration in light as well as an enhanced volumetric O2 respiration in and below the photic zone. Gross photosynthesis was largely unaffected by increasing flow velocities, whereas the O2 flux out of the photic zone, that is, net photosynthesis, increased with flow velocity. Consequently, the amount of produced O2 consumed within the biofilm decreased with increasing flow velocity. Our data indicated a close coupling of photosynthesis and respiration in biofilms, where the dissolved inorganic carbon requirement of the photosynthetic population may largely be covered by the respiration of closely associated populations of heterotrophic bacteria consuming a significant part of the photosynthetically produced oxygen and organic carbon.",
keywords = "Action spectra, Biofilms, Cyanobacteria, Diffusion, Flow, Light penetration, Microsensor, Oscillatoria sp, Photosynthesis",
author = "Michael K{\"u}hl and Glud, {Ronnie N{\o}hr} and Helle Ploug and Ramsing, {Niels Birger}",
year = "1996",
doi = "10.1111/j.0022-3646.1996.00799.x",
language = "English",
volume = "32",
pages = "799--812",
journal = "Journal of Phycology",
issn = "0022-3646",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Microenvironmental control of photosynthesis and photosynthesis-coupled respiration in an epilithic cyanobacterial biofilm

AU - Kühl, Michael

AU - Glud, Ronnie Nøhr

AU - Ploug, Helle

AU - Ramsing, Niels Birger

PY - 1996

Y1 - 1996

N2 - The photosynthetic performance of an epilithic cyanobacterial biofilm was studied in relation to the in situ light field by the use of combined microsensor measurements of O2, photosynthesis, and spectral scalar irradiance. The high density of the dominant filamentous cyanobacteria (Oscillatoria sp.) embedded in a matrix of exopolymers and bacteria resulted in a photic zone of <0.7 mm. At the biofilm surface, the prevailing irradiance and spectral composition were significantly different from the incident light. Multiple scattering led to an intensity maximum for photic light (400-700 nm) of ca. 120% of incident quantum irradiance at the biofilm surface. At the bottom of the euphotic zone in the biofilm, light was attenuated strongly to <5-10% of the incident surface irradiance. Strong spectral signals from chlorophyll a (440 and 675 nm) and phycobilins (phycoerythrin 540-570 nm, phycocyanin 615-625 nm) were observed as distinct maxima in the scalar irradiance attenuation spectra in the upper 0.0-0.5 mm of the biofilm. The action spectrum for photosynthesis in the cyanobacterial layer revealed peak photosynthetic activity at absorption wavelengths of phycobilins, whereas only low photosynthesis rates were induced by light absorption of carotenoids (450-550 nm). Respiration rates in light- and dark-incubated biofilms were determined using simple flux calculations on measured O2 concentration profiles and photosynthetic rates. A significantly higher a real O2 consumption was found in illuminated biofilms than in dark-incubated biofilms. Although photorespiration accounted for part of the increase, the enhanced areal O2 consumption of illuminated biofilms could also be ascribed to a deeper oxygen penetration in light as well as an enhanced volumetric O2 respiration in and below the photic zone. Gross photosynthesis was largely unaffected by increasing flow velocities, whereas the O2 flux out of the photic zone, that is, net photosynthesis, increased with flow velocity. Consequently, the amount of produced O2 consumed within the biofilm decreased with increasing flow velocity. Our data indicated a close coupling of photosynthesis and respiration in biofilms, where the dissolved inorganic carbon requirement of the photosynthetic population may largely be covered by the respiration of closely associated populations of heterotrophic bacteria consuming a significant part of the photosynthetically produced oxygen and organic carbon.

AB - The photosynthetic performance of an epilithic cyanobacterial biofilm was studied in relation to the in situ light field by the use of combined microsensor measurements of O2, photosynthesis, and spectral scalar irradiance. The high density of the dominant filamentous cyanobacteria (Oscillatoria sp.) embedded in a matrix of exopolymers and bacteria resulted in a photic zone of <0.7 mm. At the biofilm surface, the prevailing irradiance and spectral composition were significantly different from the incident light. Multiple scattering led to an intensity maximum for photic light (400-700 nm) of ca. 120% of incident quantum irradiance at the biofilm surface. At the bottom of the euphotic zone in the biofilm, light was attenuated strongly to <5-10% of the incident surface irradiance. Strong spectral signals from chlorophyll a (440 and 675 nm) and phycobilins (phycoerythrin 540-570 nm, phycocyanin 615-625 nm) were observed as distinct maxima in the scalar irradiance attenuation spectra in the upper 0.0-0.5 mm of the biofilm. The action spectrum for photosynthesis in the cyanobacterial layer revealed peak photosynthetic activity at absorption wavelengths of phycobilins, whereas only low photosynthesis rates were induced by light absorption of carotenoids (450-550 nm). Respiration rates in light- and dark-incubated biofilms were determined using simple flux calculations on measured O2 concentration profiles and photosynthetic rates. A significantly higher a real O2 consumption was found in illuminated biofilms than in dark-incubated biofilms. Although photorespiration accounted for part of the increase, the enhanced areal O2 consumption of illuminated biofilms could also be ascribed to a deeper oxygen penetration in light as well as an enhanced volumetric O2 respiration in and below the photic zone. Gross photosynthesis was largely unaffected by increasing flow velocities, whereas the O2 flux out of the photic zone, that is, net photosynthesis, increased with flow velocity. Consequently, the amount of produced O2 consumed within the biofilm decreased with increasing flow velocity. Our data indicated a close coupling of photosynthesis and respiration in biofilms, where the dissolved inorganic carbon requirement of the photosynthetic population may largely be covered by the respiration of closely associated populations of heterotrophic bacteria consuming a significant part of the photosynthetically produced oxygen and organic carbon.

KW - Action spectra

KW - Biofilms

KW - Cyanobacteria

KW - Diffusion

KW - Flow

KW - Light penetration

KW - Microsensor

KW - Oscillatoria sp

KW - Photosynthesis

U2 - 10.1111/j.0022-3646.1996.00799.x

DO - 10.1111/j.0022-3646.1996.00799.x

M3 - Journal article

AN - SCOPUS:0030471321

VL - 32

SP - 799

EP - 812

JO - Journal of Phycology

JF - Journal of Phycology

SN - 0022-3646

IS - 5

ER -

ID: 201684059