Pigment biomarkers and particulate carbon in the upper water column compared to the ocean interior of the northeast Atlantic

• Published in: Deep-sea research. Part I, Oceanographic research papers Oceanographic research papers, 1996-08, Vol.43 (8), p.1165-1184
• Main Authors: Llewellyn, C.A., Mantoura, R.F.C.
• Format: Article
• Language: English
• Subjects: Carbon; Earth, ocean, space; Exact sciences and technology; External geophysics; Oceanography; Oceans; Physical and chemical properties of sea water; Physics of the oceans
• ISSN: 0967-0637; 1879-0119
• DOI: 10.1016/0967-0637(96)00043-X

In situ pumps (SAPs) were used to collect particulates from the upper and interior of the ocean at 47, 56 and 60°N along the 20°W meridian in the northeast Atlantic during 1989. The particulates were analysed for carbon, chlorophylls, chlorophyll degradation products and carotenoids covering a four order of magnitude change in concentration. There was a logarithmic decline in pigment and carbon concentrations from the surface to 1000 m, below which concentrations remained constant. The gradient of the decline for chlorophyll a (chl a) appeared to be directly related to the flux of organic matter from the upper ocean. 19′-Hexanoyloxyfucoxanthin (prymnesiophtyes) and fucoxanthin (diatoms) persisted throughout the water column revealing the importance of prymnesiophytes as well as diatoms in the transfer of biogenic material into the ocean interior. At 60°N there was a two order of magnitude decrease in chl a concentrations in the ocean interior compared to the surface (1 μg chl a l −1). At 47°N, surface chl a concentrations were similar to those 60°N, but in the ocean interior there was a three order of magnitude decrease. Chlorophyll a concentrations throughout the water column and differences in the type of assessory pigment present at the four latitudes were consistent with the timing of the spring bloom at each latitude. At 60°N, we sampled at the end of the spring bloom, and fucoxanthin dominated. At 47°N, the spring bloom was over, and 19′-hexanoyloxyfucoxanthin dominated. Pheophorbide a and pyropheophorbide a were the dominant chlorophyll degradation products, with highest concentrations in the north. Pyropheophorbide a became increasingly important with depth and towards the south. At least 50% of the organic carbon in the upper ocean could not be accounted for in terms of phytoplankton, zooplankton or bacteria, and we speculate that some of the unidentified carbon is related to microzooplankton faecal material. Carbon vertical profiles did not show the large latitudinal variation of the pigments, resulting in carbon/chl a ratios in the ocean interior at 47°N (1855) being 6-fold greater than those at 60°N. The ratios reflected the more highly degraded nature of the biogenic material in the ocean interior at 47°N compared to 60°N.