A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes: Application for P vs E0(PAR) measurements in a microbial mat

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes : Application for P vs E0(PAR) measurements in a microbial mat. / Kühl, Michael; Lassen, Carsten; Revsbech, Niels Peter.

In: Aquatic Microbial Ecology, Vol. 13, No. 2, 1997, p. 197-207.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Kühl, M, Lassen, C & Revsbech, NP 1997, 'A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes: Application for P vs E0(PAR) measurements in a microbial mat', Aquatic Microbial Ecology, vol. 13, no. 2, pp. 197-207. https://doi.org/10.3354/ame013197

APA

Kühl, M., Lassen, C., & Revsbech, N. P. (1997). A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes: Application for P vs E0(PAR) measurements in a microbial mat. Aquatic Microbial Ecology, 13(2), 197-207. https://doi.org/10.3354/ame013197

Vancouver

Kühl M, Lassen C, Revsbech NP. A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes: Application for P vs E0(PAR) measurements in a microbial mat. Aquatic Microbial Ecology. 1997;13(2):197-207. https://doi.org/10.3354/ame013197

Author

Kühl, Michael ; Lassen, Carsten ; Revsbech, Niels Peter. / A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes : Application for P vs E0(PAR) measurements in a microbial mat. In: Aquatic Microbial Ecology. 1997 ; Vol. 13, No. 2. pp. 197-207.

Bibtex

@article{c4e784cbfeb24b15b4fc982bc1b474c2,
title = "A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes: Application for P vs E0(PAR) measurements in a microbial mat",
abstract = "A simple portable light meter for use with fiber-optic microprobes was developed. The meter has a flat spectral quantum responsivity for 400 to 700 nm light (photosynthetically available radiation, PAR). With scalar irradiance microprobes connected to the meter, it was possible to directly measure photosynthetically available quantum scalar irradiance, E0(PAR), at <100 μm spatial resolution and over a dynamic range from <1 to >1300 μmol photons m-2 s-1. We used the new instrument for scalar irradiance measurements in microbial mats from a freshwater lake (Lake Stigsholm, Denmark) and from a hypersaline pond (Eilat, Israel). Combined measurements of quantum scalar irradiance by fiber-optic microprobes and oxygenic photosynthesis by oxygen microelectrodes made it possible to measure gross photosynthesis as a function of the prevailing scalar irradiance (P vs E0 curves) at distinct depths within an undisturbed hypersaline microbial mat of immotile unicellular cyanobacteria (Aphanothece spp.). Intense photosynthesis by the cyanobacteria resulted in oxygen supersaturation and a 10-fold increase of oxygen penetration in the illuminated mat (zmax = 2.5 mm) as compared to the oxygen penetration in dark incubated mats (zmax = 0.2 to 0.3 mm). The mat changed from a net oxygen consuming to a net oxygen producing community at an oxygen compensation irradiance of 14 to 26 μmol photons m-2 s-1. The photic zone of the microbial mat was only 0.6 mm deep due to a high attenuation of PAR. The diffuse vertical attenuation coefficient of E0(PAR) was K0(PAR) = 6.3 mm-1. In the upper 0.2 mm of the microbial mat photosynthesis was photoinhibited at scalar irradiance above 200 μmol photons m-2 s-1. At 0.3 mm the strong light attenuation prevented inhibition in deeper layers of the microbial mat and photosynthesis approached saturation at 35 μmol photons m-2 s-1. In the lower part of the photic zone, photosynthesis increased linearly with E0(PAR). Areal gross photosynthesis exhibited no photoinhibition at high irradiance and started to approach saturation above a downwelling quantum irradiance of 97 μmol photons m-2 s-1.",
keywords = "Calibration, Cyanobacteria, Light meter, Light penetration, Microbial mat, Microsensor, Photoinhibition, Photosynthesis, Scalar irradiance",
author = "Michael K{\"u}hl and Carsten Lassen and Revsbech, {Niels Peter}",
year = "1997",
doi = "10.3354/ame013197",
language = "English",
volume = "13",
pages = "197--207",
journal = "Aquatic Microbial Ecology",
issn = "0948-3055",
publisher = "Inter research",
number = "2",

}

RIS

TY - JOUR

T1 - A simple light meter for measurements of PAR (400 to 700 nm) with fiber-optic microprobes

T2 - Application for P vs E0(PAR) measurements in a microbial mat

AU - Kühl, Michael

AU - Lassen, Carsten

AU - Revsbech, Niels Peter

PY - 1997

Y1 - 1997

N2 - A simple portable light meter for use with fiber-optic microprobes was developed. The meter has a flat spectral quantum responsivity for 400 to 700 nm light (photosynthetically available radiation, PAR). With scalar irradiance microprobes connected to the meter, it was possible to directly measure photosynthetically available quantum scalar irradiance, E0(PAR), at <100 μm spatial resolution and over a dynamic range from <1 to >1300 μmol photons m-2 s-1. We used the new instrument for scalar irradiance measurements in microbial mats from a freshwater lake (Lake Stigsholm, Denmark) and from a hypersaline pond (Eilat, Israel). Combined measurements of quantum scalar irradiance by fiber-optic microprobes and oxygenic photosynthesis by oxygen microelectrodes made it possible to measure gross photosynthesis as a function of the prevailing scalar irradiance (P vs E0 curves) at distinct depths within an undisturbed hypersaline microbial mat of immotile unicellular cyanobacteria (Aphanothece spp.). Intense photosynthesis by the cyanobacteria resulted in oxygen supersaturation and a 10-fold increase of oxygen penetration in the illuminated mat (zmax = 2.5 mm) as compared to the oxygen penetration in dark incubated mats (zmax = 0.2 to 0.3 mm). The mat changed from a net oxygen consuming to a net oxygen producing community at an oxygen compensation irradiance of 14 to 26 μmol photons m-2 s-1. The photic zone of the microbial mat was only 0.6 mm deep due to a high attenuation of PAR. The diffuse vertical attenuation coefficient of E0(PAR) was K0(PAR) = 6.3 mm-1. In the upper 0.2 mm of the microbial mat photosynthesis was photoinhibited at scalar irradiance above 200 μmol photons m-2 s-1. At 0.3 mm the strong light attenuation prevented inhibition in deeper layers of the microbial mat and photosynthesis approached saturation at 35 μmol photons m-2 s-1. In the lower part of the photic zone, photosynthesis increased linearly with E0(PAR). Areal gross photosynthesis exhibited no photoinhibition at high irradiance and started to approach saturation above a downwelling quantum irradiance of 97 μmol photons m-2 s-1.

AB - A simple portable light meter for use with fiber-optic microprobes was developed. The meter has a flat spectral quantum responsivity for 400 to 700 nm light (photosynthetically available radiation, PAR). With scalar irradiance microprobes connected to the meter, it was possible to directly measure photosynthetically available quantum scalar irradiance, E0(PAR), at <100 μm spatial resolution and over a dynamic range from <1 to >1300 μmol photons m-2 s-1. We used the new instrument for scalar irradiance measurements in microbial mats from a freshwater lake (Lake Stigsholm, Denmark) and from a hypersaline pond (Eilat, Israel). Combined measurements of quantum scalar irradiance by fiber-optic microprobes and oxygenic photosynthesis by oxygen microelectrodes made it possible to measure gross photosynthesis as a function of the prevailing scalar irradiance (P vs E0 curves) at distinct depths within an undisturbed hypersaline microbial mat of immotile unicellular cyanobacteria (Aphanothece spp.). Intense photosynthesis by the cyanobacteria resulted in oxygen supersaturation and a 10-fold increase of oxygen penetration in the illuminated mat (zmax = 2.5 mm) as compared to the oxygen penetration in dark incubated mats (zmax = 0.2 to 0.3 mm). The mat changed from a net oxygen consuming to a net oxygen producing community at an oxygen compensation irradiance of 14 to 26 μmol photons m-2 s-1. The photic zone of the microbial mat was only 0.6 mm deep due to a high attenuation of PAR. The diffuse vertical attenuation coefficient of E0(PAR) was K0(PAR) = 6.3 mm-1. In the upper 0.2 mm of the microbial mat photosynthesis was photoinhibited at scalar irradiance above 200 μmol photons m-2 s-1. At 0.3 mm the strong light attenuation prevented inhibition in deeper layers of the microbial mat and photosynthesis approached saturation at 35 μmol photons m-2 s-1. In the lower part of the photic zone, photosynthesis increased linearly with E0(PAR). Areal gross photosynthesis exhibited no photoinhibition at high irradiance and started to approach saturation above a downwelling quantum irradiance of 97 μmol photons m-2 s-1.

KW - Calibration

KW - Cyanobacteria

KW - Light meter

KW - Light penetration

KW - Microbial mat

KW - Microsensor

KW - Photoinhibition

KW - Photosynthesis

KW - Scalar irradiance

U2 - 10.3354/ame013197

DO - 10.3354/ame013197

M3 - Journal article

AN - SCOPUS:0000830474

VL - 13

SP - 197

EP - 207

JO - Aquatic Microbial Ecology

JF - Aquatic Microbial Ecology

SN - 0948-3055

IS - 2

ER -

ID: 201683961