0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology

Phytoplankton cell size is believed to be closely regulated by the nutrient regime of water masses in the western North Atlantic Ocean. Since particle size affects attenuation of light in ocean water, we argue that a bridge between classical ocean optics and microbial ecology has formed whereby the...

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Main Authors: Charles S. Yentsch, David A. Phinney
Other Authors: The Pennsylvania State University CiteSeerX Archives
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Language:English
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.556.3498
http://www.aslo.org/lo/toc/vol_34/issue_8/1694.pdf
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spelling ftciteseerx:oai:CiteSeerX.psu:10.1.1.556.3498 2023-05-15T17:31:40+02:00 0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology Charles S. Yentsch David A. Phinney The Pennsylvania State University CiteSeerX Archives application/pdf http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.556.3498 http://www.aslo.org/lo/toc/vol_34/issue_8/1694.pdf en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.556.3498 http://www.aslo.org/lo/toc/vol_34/issue_8/1694.pdf Metadata may be used without restrictions as long as the oai identifier remains attached to it. http://www.aslo.org/lo/toc/vol_34/issue_8/1694.pdf text ftciteseerx 2016-01-08T11:47:39Z Phytoplankton cell size is believed to be closely regulated by the nutrient regime of water masses in the western North Atlantic Ocean. Since particle size affects attenuation of light in ocean water, we argue that a bridge between classical ocean optics and microbial ecology has formed whereby the physics of ocean color must include consideration of ecological factors important to the diversity of phytoplankton species. Observations of the specific absorption coefficient, a*, have been made during 10 oceanographic cruises in the western North Atlantic. The range in Chl a concentration for ocean samples from the various water masses in this region was 0.1-8.0 pg liter-l. Diffuse attenuation spectra of particles measured by a glass-fiber filter technique show strong correlations between extracted chlorophyll and blue (440 nm) or red (670 nm) absorption. Of the two, a*440 is the most variable. Average specific absorption coefficients are calculated to be 0.049 m2 mg- ’ at 440 nm and 0.028 at 670 nm, but both relationships are seen to be nonlinear. The nonlinearity observed is attributed to differences in cell size “packaging ” within natural phytoplankton populations. Variation in cell size and a * are primarily related to the availability of nitrate-N. In addition, other factors contribute to the variability in a*440, such as detritus and short wavelength UV-absorbing pigments. Particles that scatter and absorb light in the sea come from various sources; how-ever, a major source in the open ocean is primary production. Changes in optical characteristics of water masses are now re-lated to biochemical processes (Pak et al. 198 8; Mitchell and Kiefer 1988a, b; Morel Text North Atlantic Unknown
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description Phytoplankton cell size is believed to be closely regulated by the nutrient regime of water masses in the western North Atlantic Ocean. Since particle size affects attenuation of light in ocean water, we argue that a bridge between classical ocean optics and microbial ecology has formed whereby the physics of ocean color must include consideration of ecological factors important to the diversity of phytoplankton species. Observations of the specific absorption coefficient, a*, have been made during 10 oceanographic cruises in the western North Atlantic. The range in Chl a concentration for ocean samples from the various water masses in this region was 0.1-8.0 pg liter-l. Diffuse attenuation spectra of particles measured by a glass-fiber filter technique show strong correlations between extracted chlorophyll and blue (440 nm) or red (670 nm) absorption. Of the two, a*440 is the most variable. Average specific absorption coefficients are calculated to be 0.049 m2 mg- ’ at 440 nm and 0.028 at 670 nm, but both relationships are seen to be nonlinear. The nonlinearity observed is attributed to differences in cell size “packaging ” within natural phytoplankton populations. Variation in cell size and a * are primarily related to the availability of nitrate-N. In addition, other factors contribute to the variability in a*440, such as detritus and short wavelength UV-absorbing pigments. Particles that scatter and absorb light in the sea come from various sources; how-ever, a major source in the open ocean is primary production. Changes in optical characteristics of water masses are now re-lated to biochemical processes (Pak et al. 198 8; Mitchell and Kiefer 1988a, b; Morel
author2 The Pennsylvania State University CiteSeerX Archives
format Text
author Charles S. Yentsch
David A. Phinney
spellingShingle Charles S. Yentsch
David A. Phinney
0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology
author_facet Charles S. Yentsch
David A. Phinney
author_sort Charles S. Yentsch
title 0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology
title_short 0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology
title_full 0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology
title_fullStr 0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology
title_full_unstemmed 0 1989, by the American Society of Limnology and Oceanography, Inc. A bridge between ocean optics and microbial ecology
title_sort 0 1989, by the american society of limnology and oceanography, inc. a bridge between ocean optics and microbial ecology
url http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.556.3498
http://www.aslo.org/lo/toc/vol_34/issue_8/1694.pdf
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