Abstract

Abstract. The Labrador Sea is an ideal region to study the biogeographical, physiological, and biogeochemical implications of phytoplankton community composition due to sharp transitions between distinct water masses across its shelves and central basin. We have investigated the multi-year (2005–2014) distributions of late spring and early summer (May to June) phytoplankton communities in the various hydrographic settings of the Labrador Sea. Our analysis is based on pigment markers (using CHEMTAX analysis), and photophysiological and biogeochemical characteristics associated with each phytoplankton community. Diatoms were the most abundant group, blooming first in shallow mixed layers of haline-stratified Arctic shelf waters. Along with diatoms, chlorophytes co-dominated at the western end of the section (particularly in the polar waters of the Labrador Current (LC)), whilst Phaeocystis co-dominated in the east (modified polar waters of the West Greenland Current (WGC)). Pre-bloom conditions occurred in deeper mixed layers of the central Labrador Sea in May, where a mixed assemblage of flagellates (dinoflagellates, prasinophytes, prymnesiophytes, particularly coccolithophores, and chrysophytes/pelagophytes) occurred in low-chlorophyll areas, succeeding to blooms of diatoms and dinoflagellates in thermally stratified Atlantic waters in June. Light-saturated photosynthetic rates and saturation irradiance levels were highest at stations where diatoms were the dominant phytoplankton group ( > 70 % of total chlorophyll a), as opposed to stations where flagellates were more abundant (from 40 up to 70 % of total chlorophyll a). Phytoplankton communities from the WGC (Phaeocystis and diatoms) had lower light-limited photosynthetic rates, with little evidence of photoinhibition, indicating greater tolerance to a high light environment. By contrast, communities from the central Labrador Sea (dinoflagellates and diatoms), which bloomed later in the season (June), appeared to be more sensitive to high light levels. Ratios of accessory pigments (AP) to total chlorophyll a (TChl a) varied according to phytoplankton community composition, with polar phytoplankton (cold-water related) having lower AP : TChl a. Polar waters (LC and WGC) also had higher and more variable particulate organic carbon (POC) to particulate organic nitrogen (PON) ratios, suggesting the influence of detritus from freshwater input, derived from riverine, glacial, and/or sea ice meltwater. Long-term observational shifts in phytoplankton communities were not assessed in this study due to the short temporal frame (May to June) of the data. Nevertheless, these results add to our current understanding of phytoplankton group distribution, as well as an evaluation of the biogeochemical role (in terms of C : N ratios) of spring phytoplankton communities in the Labrador Sea, which will assist our understanding of potential long-term responses of phytoplankton communities in high-latitude oceans to a changing climate.

Highlights

  • Marine phytoplankton form a taxonomically and functionally diverse group, where communities are structured by a variety of factors, including nutrient and light availability, predation and competition for resources (Litchman and Klausmeier, 2008)

  • The purpose of this study was to answer the following questions: were there distinct phytoplankton communities in the Labrador Sea and if so, what were their main constituents? How did spatial and temporal variability in environmental factors explain the phytoplankton community distribution and composition? What were the linkages between community composition and variability in both particulate matter stoichiometry (i.e. C : N ratios) and photophysiological traits across the Labrador Sea?

  • Our results provide a geographical description of the phytoplankton community structure in spring and early summer surface waters of the Labrador Sea based on pigment data and CHEMTAX analysis from over a decade of sampling

Read more

Summary

Introduction

Marine phytoplankton form a taxonomically and functionally diverse group, where communities are structured by a variety of factors, including nutrient and light availability, predation and competition for resources (Litchman and Klausmeier, 2008). Such environmental heterogeneity creates biogeographical patterns of abundance, composition, traits, and diversity of phytoplankton communities in the global ocean (Barton et al, 2013; Follows et al, 2007; Hays et al, 2005). Phytoplankton communities within a biogeographical region are subject to similar environmental conditions, such as temperature (Bouman et al, 2003), nutrient concentration (Browning et al, 2014), and irradiance (Arrigo et al, 2010). Patterns of phytoplankton stoichiometry may be consistent phylogenetically within higher taxonomic levels (Ho et al, 2003; Quigg et al, 2003); stoichiometry varies according to nutrient supply ratios (Bertilsson et al, 2003; Rhee, 1978) and phenotypically within species of the same population (Finkel et al, 2006)

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call