Artigo Revisado por pares

Phytoplankton pigment chemotaxonomy of the northeastern Atlantic

2001; Elsevier BV; Volume: 48; Issue: 4-5 Linguagem: Inglês

10.1016/s0967-0645(00)00098-9

ISSN

1879-0100

Autores

Stuart W. Gibb, Denise Cummings, Xabier Irigoien, Ray Barlow, R. Fauzi, C. Mantoura,

Tópico(s)

Ocean Acidification Effects and Responses

Resumo

Phytoplankton pigment distributions were studied between 62 and 37°N in the northeastern Atlantic as a component of the NERC PRIME programme. At the northern end of the transect, waters were characterised by a surface chlorophyll a (CHLa) maximum of 500–700ngl−1 (0–40m). At the southern end, surface waters were virtually devoid of nutrients (NO3−<0.5μM,NH4+<50nM), and surface CHLa concentrations were <50ngl−1. At 37°N a well-defined deep CHLa maximum (DCM) was recorded between 60 and 100 m (∼350ngl−1). Highest concentrations of CHLa (1500μgl−1) were measured in the surface mixed layer to the south of a well-defined salinity and temperature front at 52.5°N. Overall, 19′-hexanoyloxyfucoxanthin (HEX, up to 1120ngl−1) was the dominant accessory pigment, although zeaxanthin (ZEA) was the major accessory pigment at 37°N. Conversion of pigment data into quantitative estimates of algal class abundances indicated the composition of phytoplankton population was relatively stable in surface waters between 62 and 52.5°N: Prymnesiophytes were the most abundant class, contributing a mean of 38% of the total CHLa, while cryptophytes (20%), chlorophytes (14%) and diatoms (15%) contributed the bulk of the remaining CHLa. Together, these four classes accounted for 79–92% of the total CHLa in this section of the transect. Immediately south of the front (52–50°N), prymnesiophytes contributed approximately half of the total CHLa, while south of 50°N there was a shift to a population dominated by cyanobacteria and prochlorophytes, which together accounted for a mean of 53% of the measured total CHLa at 37°N. At 37°N the contribution of cyanobacteria to total CHLa declined significantly with depth, and the DCM was dominated by prochlorophytes, prymnesiophytes and cryptophytes. Below the DCM, chrysophytes were the most abundant class of phytoplankton, contributing 30% of the total CHLa, with prymnesiophytes, prochlorophytes and cryptophytes also making significant contributions. The contribution of prymnesiophytes to total CHLa was found to be relatively stable throughout the water column (23%, SD 3%). Although highest concentrations of divinyl chlorophyll a (dvCHLa) were recorded in the DCM, the contribution of dvCHLa to total CHLa (dvCHLa + CHLa) was only 21–26% here compared to up to 48% (mean=33±9.6%) in surface waters. The ratio of [dvCHLa]: prochlorophyte biomass increased from 10ngμgC−1 in the surface 40 m to 56.9ngμgC−1 between 50 and 100 m. This corresponded to a rise in cellular dvCHLa from 0.215 to 1.83fgcell−1 and thus significant photo-adaptation with depth. Hence, a component of the DCM fluorescence and pigment signals is the result of increased cellular pigmentation rather than from increases in biomass alone. On the basis of inter-pigment ratios, we suggest that the DCM was dominated by an Atlantic strain of prochlorophytes, adapted to lower light levels, while the surface oligotrophic layer was composed of a mixed population of both Atlantic and a higher light adapted Mediterranean strain. Correlation studies indicated the potential of CHLa, fucoxanthin (FUC) and HEX to serve as respective proxy markers of POC and the biominerals silicate (SiO2) and calcite (CaCO3) in surface waters (r=0.49–0.78,p<0.001) and in depth profiles at northern latitudes (59°N,r=0.74–0.75,p<0.001). However, poor correlations were observed in depth profiles at the southern end of the transect.

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