Spatial variations in the chlorophyll-specific absorption coefficients of phytoplankton and photosynthetically active pigments in the equatorial Pacific

被引:90
作者
Allali, K [1 ]
Bricaud, A [1 ]
Claustre, H [1 ]
机构
[1] UNIV PARIS 06,VILLEFRANCHE MER,FRANCE
来源
JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS | 1997年 / 102卷 / C6期
关键词
D O I
10.1029/97JC00380
中图分类号
P7 [海洋学];
学科分类号
0707 ;
摘要
Chlorophyll-specific absorption coefficients of particles, a(p)*(lambda), and of length amplification effect was derived from field measurements. Then a decomposition technique using the high-performance liquid chromatography pigment information and taking into account the package effect was used to partition a(ph)* into the contributions of photosynthetic pigments (a(ps)*) and nonphotosynthetic pigments (a(nps)*). Both a(ph)*, and a values were observed to decrease from the oligotrophic waters of the subequatorial nps area (13 degrees-1 degrees S) to the mesotrophic waters of the equatorial area (1 degrees S-1 degrees N) and from the surface to deep waters. The a(ph)* variations were primarily, but not exclusively, caused by changes in the concentrations of nonphotosynthetic pigments. The level of pigment packaging was also variable both horizontally and vertically, as a result of changes in populations and photoacclimation. In comparison with a(ph)*, a(ps)* exhibited a reduced range of variation with depth and along the latitudinal gradient. The variations in a(ps)* originating from the package effect were partly compensated by variations in the concentrations of photosynthetic pigments. We extended this analysis to include data collected in other areas with different trophic states. The a(ps)* values varied over a factor of 4 at 440 nm, instead of 8 for a(ph)*, for chlorophyll a concentrations covering 2 orders of magnitude (0.02-2 mg m(-3)). In agreement with a previous study performed off California with a different method [Sosik and Mitchell, 1995], we conclude that a(ps)* is less dependent on environmental parameters than a(ps)*. In addition, our results provide evidence that the variability in a(ps)* cannot be neglected. The use of a(ps)* instead of a(ph)* in light-photosynthesis models (in conjunction with a quantum yield for carbon fixation defined with respect to the photosynthetically active absorbed amount of quanta) presents the advantage of removing the variability associated with nonphotosynthetic pigments.
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收藏
页码:12413 / 12423
页数:11
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