Deep Sea Research Part II: Topical Studies in Oceanography
Distribution of phytoplankton and other protists in the North Water
Introduction
Phytoplankton species have been reported to be associated with different water masses for at least 120 years (Castracane, 1884; Braarud and Klem, 1931; Grøntved and Seidenfaden, 1938; Hasle, 1990). Species composition of protist communities is functionally important because it is thought to influence the export capacity of oceans (Goldman, 1993; Dugdale et al., 1990; Legendre and Rassoulzadegan, 1996) and zooplankton growth rate (Starr et al., 1999). The North Water is a biologically rich polynya, isolated from the temperate oceanic provinces and, due to its high latitude, characterized by extreme seasonal fluctuations. The area is also nutrient-rich and contains a number of distinct physical water masses that intermingle to a greater or lesser extent over the summer growing season and over different regions of the polynya (Bâcle et al., 2002). Grøntved and Seidenfaden (1938) summarized all records of net phytoplankton distribution west of Greenland, between 1850 and 1928. The North Water, however, had not been sampled extensively for phytoplankton and other protists over the past 70 years.
The International North Water Polynya Study (NOW) provided an opportunity to investigate general phytoplankton and other protist distribution over the spring and early summer in 1998. Older studies had emphasized the biogeography of net plankton; no information was available on the relative importance of different groups of diatoms compared to ciliates, dinoflagellates, and flagellates in terms of total standing biomass carbon over the growth season or within different regions. In many oceanic waters picoplankton (0.2–2 μm) and nanoplankton (2–20 μm) contribute substantially more to total particulate organic carbon than do large net plankton (Li and Wood, 1988; Booth et al., 1993; Sanders et al., 2000). In the North Water the relative importance of the larger microplankton or net-plankton (20–200 μm) compared to smaller nanoplankton (2–20 μm) had not been investigated.
Taxonomic details on the distribution of small flagellates, especially prymnesiophytes, prasinophytes, and choanoflagellates, are given in Gammelgaard (2000). A more detailed description of the spatial and temporal distribution of Chaetoceros socialis, a dominant diatom found during 1998, is given in Booth et al. (2002). The aims of the present study were two-fold: to quantify the contribution of different types of large and colony-forming diatoms, reported from net tows taken in the North Water since 1876; and to compare the biomass of these large diatoms to the contribution of alveolates (ciliates and dinoflagellates) and the smaller and more taxonomically diverse nanoplankton for the various regions of the polynya, as influenced by different water masses (Bâcle et al., 2002).
Section snippets
Methods
Samples were collected on board the Canadian Coast Guard icebreaker, Pierre Radisson, during four legs of the 1998 NOW expedition that corresponded to the months of April, May, June, and July. Water samples were collected using a rosette sampler (General Oceanics) equipped with 10-l Niskin type bottles and a Falmouth Scientific Instruments Integrated CTD. A few additional samples and measurements were taken using 5-l Niskin bottles on a line and a SeaBird-25 CTD. Samples for phytoplankton and
Polynyawide
Diatoms dominated in the North Water over the 4 months of intensive sampling in 1998, accounting overall for 70% of total biomass of the community of phytoplankton and other protists. Over 40% of the total biomass belonged to the Thalassiosira spp./Porosira glacialis group, diatoms that form long chains of relatively large cells. Dinoflagellates and ciliates comprised nearly 24% of total biomass, while smaller flagellates were responsible for less than 6%. Biomass of pico-sized cells was
Discussion
The microscopic method used in the present study to count phytoplankton and other protists (FNU method, a combination of Fluorescence, Nomarski optics and Utermöhl sedimentation; Lovejoy et al (1993), Lovejoy et al (2000)) has the advantage of making it possible to visualize the entire community using one technique. While one cannot identify every individual protist to species level, most of them can be seen to belong to a particular taxon. The Utermöhl technique (Utermöhl, 1958) has been
Acknowledgments
We extend thanks to the captains and crew of the CCGS Pierre Radisson for logistic support and to M. Roberts, B. van Hardenberg, D. Sieberg, Z.-P. Mei, B. Leblanc, B. Klein and others who ensured that samples were collected. Laboratory assistance by J. Bouchard-Roussin, P. Harle, L. Chanet and J. Guihard is gratefully acknowledged. Encouragement and comments from W.F. Vincent, B.C. Booth, H.A. Thomsen, N. Daugbjerg, T.G. Nielsen, J. Østergaard, and M. Fortier were appreciated. Funding was
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