Towards an Ecological Status Report for Phytoplankton and Microbial Plankton in the North Atlantic

Towards an Ecological Status Report for Phytoplankton and Microbial Plankton in the North Atlantic

Not to be cited without prior reference to the authors ICES CM 2011/B:02 Towards an ecological status report for phytoplankton and microbial plankton in the North Atlantic William K.W. Li1, Xosé Anxelu G. Morán2, Todd D. O’Brien3 and WGPME participants4 1Bedford Institute of Oceanography, Dartmouth, Nova Scotia, Canada, B2Y 4A2 2Instituto Español de Oceanografía, Centro Oceanográfico de Xixón, Camín de L’Arbeyal, s/n, 33212 Xixón, Spain 3National Oceanic and Atmospheric Administration, National Marine Fisheries Service, Silver Spring, Maryland 20910, USA 4Appendix 1Contact: [email protected] Abstract The ecological links between the physical environment of the ocean and the mid to upper trophic levels of pelagic food webs are the lower trophic levels comprising microbial primary producers (phytoplankton) and microbial secondary producers (bacterioplankton, heterotrophic protists). In the North Atlantic Ocean, standardized annual average anomalies of oceanic hydrography (WGOH) and of mesozooplankton (WGZE) derived from time series observations at monitoring sites located across the entire basin provide long term trends suitable for discerning climate variability and change. Here we (WGPME) describe work in progress aimed at establishing contemporaneous trends at similar scales of space and time for phytoplankton and other microbial plankton (and associated variables such as inorganic nutrients), with a view towards understanding climatic and anthropogenic signal propagation through ocean ecosystems. Preliminary analysis hints at a widespread increase in the annual average abundance of smaller phytoplankton cells that presumably may alter the flux of energy from lower to higher trophic levels. Keywords: phytoplankton, microbial plankton, ecological status, WGPME Introduction examine species, functional groups, and community The ICES Science Plan places a high priority on descriptors since microbial attributes may prove understanding the functioning of ecosystems through important for indicating systemic change. Here, we research on key topics that include climate change and report on the progress of WGPME towards an biodiversity resilience. To these ends, it is important to ecological status report for phytoplankton and microbial discern changes in distributional patterns at the species plankton in the North Atlantic. Such a report would and community levels, as well as to define indicators contribute to the observational description of lower that contain information on ecosystem attributes, trophic levels required in any ecosystem-based conditions of change, and external pressures. These are assessment of the state of the North Atlantic Ocean. the outcomes towards which the Working Group on Phytoplankton and Microbial Ecology (WGPME) are striving. Methods A perspective on changing conditions in the The cooperative research agenda for phytoplankton and world’s Large Marine Ecosystems indicate no microbial plankton is based on the successful model of significant trends in chlorophyll or primary production WGZE for the ICES zooplankton status report (O’Brien in the various LMEs of the North Atlantic, except on the et al. 2011). To date, WGPME has a collection of data East Greenland Shelf and in the Barents Sea where from 22 discrete monitoring stations. Long-term chlorophyll concentrations have been increasing records of sea surface temperature (1900-2010) and (Sherman and Hempel 2009). However, the evidence in ocean colour (1998-2010) at every monitoring site are this perspective was drawn largely from satellite ocean extracted from the Hadley Centre SST colour measurements made over a relatively short time (http://badc.nerc.ac.uk/data/hadisst/) and the duration (1998-2006). Although these findings have GlobColour (http://www.globcolour.info/) databases been considered in the context of other existing data respectively. Multidecade records (1958-2009) of (Bode et al. 2011), there remains an ongoing need to diatoms, dinoflagellates and phytoplankton colour index 1 Not to be cited without prior reference to the authors ICES CM 2011/B:02 in 40 standard geographic areas of the North Atlantic abundance has increased at 26 locations and decreased are contributed from the Continuous Plankton Recorder at 27 other locations. (CPR) database of the Sir Alister Hardy Foundation for Ocean Science (http://www.SAHFOS.org). Phytoplankton Colour Index Datasets contributed into the cooperative collection The CPR phytoplankton colour index (PCI) is a 50 year are analysed using the Coastal and Oceanic Plankton proxy for in situ chlorophyll in the top three meters of Ecology, Production, and Observation Database the water column (Batten et al. 2003). With a solitary (COPEPOD) Interactive Time-series Explorer exception, the CPR PCI shows a pan-North Atlantic (COPEPODITE, multiyear increase, with weak trends across most http://www.st.nmfs.noaa.gov/copepodite). The oceanic regions and strong trends only at sites generally extraction and analysis methods have been fully near the ocean boundaries (Fig. 4). Over all CPR areas, described (O’Brien et al. 2011). Essentially, all data PCI has increased at 39 locations and decreased at only values in a time series are converted to a unitless ratio 1 location. (anomaly) to indicate change over time relative to the long-term average (climatology). This method removes Ocean colour any seasonal signal and the resulting multiyear trend is As an indicator of upper ocean phytoplankton assessed by linear regression of the annual anomalies. chlorophyll concentration, satellite ocean colour Multiyear change in any variable is designated as (GlobCHL) shows a general pan-North Atlantic strong, weak, or non-significant according to whether multiyear increase. The trends are weak in the central the regression slope is highly significant (p < 0.01), oceanic basin but strengthen decisively at the ocean significant (p < 0.05), or not significant (p > 0.05) boundaries and coastal stations, many of which are respectively. monitored by WGZE (Fig. 5). Over all CPR areas and both WGPME and WGZE sites, ocean colour has increased at 58 locations and decreased only at 7 Results locations. Time-series data analysis and visualisation For each microbial variable, the objectives are to Cross comparison establish the climatology, to describe the interannual At the WGPME sites examined to date, a visual variability, and to discern any multiyear trend. An cross-comparison of the variables indicates a striking example is shown for the abundance (cells l-1) of pattern. Bulk phytoplankton biomass (GlobCHL) is diatoms in the Bay of Fundy, Canada (Fig. 1). Here, increasing at an overwhelming majority of the sites diatoms exhibit an annual cycle characterised by a broad (20/22=91%), and this is matched only by the summer peak and a multiyear increase in annual average phytoflagellates and picophytoplankton (11/12=92%), abundance that is highly significant (p<0.01). The same but not the diatoms (10/14=71%), the dinoflagellates presentation of results for data from other sites can be (8/13=62%), nor the bacteria (5/9=56%). There are too found at http://WGPME.net few measurements of coccolithophores even for a qualitative assessment. Since many of the rates of Diatoms change are not statistically significant, this putative Multiyear diatom change is weak across the oceanic pattern needs to be re-examined with additional data North Atlantic basin. The trend is generally negative in from other sites and longer time series at the existing the east and positive in the west. Closer to, and adjacent sites. As it stands, there is a suggestion of coherent to the coasts of Europe and Canada, diatom change increases in annual average concentration of chlorophyll appears strong. The trend is generally positive except in and the annual average abundance of smaller proximity to the English Channel and the Bay of Biscay phytoplankton cells. (Fig. 2). Over all CPR areas and WGPME sites, diatom abundance has increased at 27 locations and decreased at 27 other locations. Discussion In working towards a pan-North Atlantic survey of the Dinoflagellates state of phytoplankton and microbial plankton change, Multiyear change in dinoflagellate abundance is we recognise the importance of seasonality in ecological similarly weak across the oceanic basin, generally being development and the likelihood of phenological negative in the east and positive in the west. As with adjustments to climate change and variability (Cloern diatoms, strong changes in dinoflagellates are evident and Jassby 2008, Winder and Cloern 2010). However only closer to and adjacent to the coasts (Fig. 3). Over at present, there are insufficient fixed stations that are all CPR areas and WGPME sites, dinoflagellate sampled at a frequency adequate to yield a robust pan- Atlantic pattern of phenological change. Arguably, high 2 Not to be cited without prior reference to the authors ICES CM 2011/B:02 turnover rate microbiota such as phytoplankton and the strongest increase in GlobCHL is evident (Fig. 5). bacteria need to be sampled at sub-monthly frequency Furthermore, it should not be expected that a linear for such a purpose. Our major current effort therefore is model for multiyear change is entirely appropriate since focused on deseasonalised indicators of long-term trophic interactions are non-linear and feedback can change. cause system oscillations (Frank et al. 2011). Preliminary results indicate a pan-North Atlantic With the data at hand, it appears that the increase in increase in bulk

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