Diatom distributions in northern North Pacific surface sediments and their relationship to modern environmental variables
Introduction
Reliable data sets of diatom species composition in ocean surface sediments are widely used for paleoceanographic reconstruction in the Southern Ocean (e.g. Zielinski and Gersonde, 1997, Crosta et al., 1998, Zielinski et al., 1998, Esper and Gersonde, 2014) and in the North Atlantic Ocean (e.g. Koç Karpuz and Schrader, 1990). In contrast, only a few investigations were published in the North Pacific decades ago (Kanaya and Koizumi, 1966, Jousé et al., 1971, Sancetta, 1979, Sancetta, 1981, Sancetta, 1982). Recent studies are either based on sparse samples (e.g. Kazarina and Yushina, 1999) or focus on minor regions (e.g. Shiga and Koizumi, 2000 and Tsoy et al., 2009 on the Sea of Okhotsk; Lopes et al., 2006 on coastal North America). The pioneer statistical analysis based on diatom species from surface samples of the entire North Pacific was done by Sancetta (1979). However, only few samples from the Bering Sea, especially from the Bering Shelf, which is covered by sea ice seasonally, were included in her study. Later work expanded the data set in the marginal seas (Sancetta, 1981) and the subarctic Pacific (Sancetta and Silvestri, 1986).
As one of the High Nutrient Low Chlorophyll (HNLC) regions, the North Pacific plays a role in controlling the glacial–interglacial atmospheric CO2 concentration variability by plankton productivity shifts, which are limited by iron availability, and by ocean stratification, which may reduce CO2 leak from deep ocean to atmosphere (Sigman et al., 2004, Haug et al., 2005, Jaccard et al., 2005). Furthermore, the atmospheric vapor and water flow from the North Pacific through the Bering Strait to the Arctic and hence the North Atlantic may stabilize the global climate variability by the salinity and heat balance (Keigwin and Cook, 2007). Thus, in order to understand the North Pacific's role in shaping global climatic and oceanographic changes, the history of paleo-sea-surface-temperature and winter sea ice distribution is of vital importance (e.g. Gebhardt et al., 2008, Max et al., 2012). Therefore, a high quality and comprehensive diatom based data set is needed for paleoceanographic reconstruction, due to the restricted occurrence of calcareous fossils and hence reconstructions based on corresponding geochemical proxies in this area.
In this paper, we present the diatom distribution in northern North Pacific sediments, including the Sea of Okhotsk and the Bering Sea. In total 422 surface samples, including 263 samples from Sancetta and Silvestri (1986) are studied here, covering the Subarctic Front system (Fig. 1a). Statistical analysis, such as Q-mode analysis and Canonical Correspondence Analysis, is applied to the diatom data set, in order to reveal the relationships between the diatom distribution and the environmental variables (e.g. sea surface temperatures, sea ice concentration, salinities, nutrients, mixed layer depths) and to detect the primary factors which determine the diatom species and their abundance distributions in the North Pacific.
Section snippets
North Pacific open ocean
The northern North Pacific open ocean can be subdivided by the Subarctic Front into the Subarctic Gyre (Dodimead et al., 1963) and the northern part of the Subtropical Gyre (e.g. Qiu, 2002; Fig. 1b). The Subarctic Front, located between 40°N and 44°N in the western and central North Pacific, is characterized by an abrupt change in temperature and salinity where the cold and fresh water of the subarctic gyre from the north meets the warm and salty subtropical water to the south (Yuan and Talley,
Material
A total of 422 surface sediment samples were recovered from the northern North Pacific including the Bering Sea and the Sea of Okhotsk, covering an area between 140°E–120°W and 30°N–70°N (Fig. 1a). Among them, 263 samples (named as SanSamp hereafter) were from a former study by Sancetta and Silvestri (1986). The other 159 surface sediment samples, studied at Alfred-Wegener-Institute (named as AWISamp hereafter), were collected during cruises INOPEX (Gersonde, 2012), KALMAR (Dullo, et al., 2009
Diatom distribution
The biogeographic distribution of 38 diatom species and species groups from 422 surface samples was investigated and mapped. Most of the species show clear distribution patterns corresponding to environmental variables, mainly the surface temperatures and the sea ice distribution. Species such as Actinocyclus octonarius, Alveus marinus, Azpeitia nodulifera, Hemidiscus cuneiformis, Rhizosolenia bergonii, R. setigera and Thalassiosira leptopus are only found south of the Subarctic Front, while
Total diatom peak flux
In order to summarize the seasonal signals preserved in the surface sediments, we compiled the monthly total diatom flux data from ten sediment traps located in the North Pacific (Fig. 1a) based on previous studies (Takahashi, 1997, Tsoy and Wong, 1999, Onodera et al., 2005, Onodera and Takahashi, 2009).
Monthly total diatom peak flux mostly appears in April with two minor occurrences in August and October (Fig. 8). Long period sediment trap results reveal a total diatom flux with spring and
Conclusions
This study documents the diatom distribution in surface sediments of the northern North Pacific. Thirty-eight diatom species from 422 surface samples throughout the area show a clear distribution pattern.
Three assemblages are distinguished by Q-mode factor analysis, representing different water masses. The Arctic Assemblage, which is restricted to the area covered by sea ice seasonally, is dominated by sea ice related diatoms (e.g. F. cylindrus, F. oceanica) and cold water species (e.g. B.
Acknowledgements
This paper is a contribution to the INOPEX (Innovative NOrth Pacific EXperiment) project funded by the Bundesministerium für Bildung und Forschung (the German Ministry of Education and Research). Gerald H. Haug from Potsdam Universität and ETH Zürich is thanked for the financial funding for J. Ren. Surface samples were taken from several cruises, e.g. INOPEX, KALMAR, KOMEX. We thank the scientific and technical staff on shipboard. We would like to acknowledge Maryse Henry and Anne de Vernal
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