K. E. Frey1, J. C. Comiso2, L. W. Cooper3, L. B. Eisner4,
R. R. Gradinger5, J. M. Grebmeier3, J. -É. Tremblay6
1Graduate School of Geography, Clark University, Worcester, MA, USA
2Cryospheric Sciences Laboratory, NASA Goddard Space Flight Center, Greenbelt, MD, USA
3Chesapeake Biological Laboratory, University of Maryland Center for Environmental Science, Solomons, MD, USA
4Alaska Fisheries Science Center, NOAA, Seattle, WA, USA
5UiT, The Arctic University of Norway, Tromsø, Norway
6Québec-Océan and Takuvik, Biology Department, Université Laval, Québec City, QC, Canada
(See erratum, published in 2021)
- Estimates of ocean primary productivity via satellite observations showed widespread positive (increasing) anomalies for 2017 (relative to the 2003-2016 mean) for all regions, with the most pronounced overall trends over the years 2003-2017 occurring in the Barents Sea and Eurasian Arctic regions.
- The regional distribution of positive (negative) anomalies in chlorophyll-a concentrations can often be associated with a relatively early (late) breakup of the sea ice cover.
- During May 2017, strong positive anomalies in chlorophyll-a concentrations occurred in the northwestern Bering Sea and in the southeastern Chukchi Sea off the coast of Point Hope, while widespread negative anomalies occurred in the Barents Sea. Negative anomalies for 2017 were also prevalent across broad areas of the Kara and Laptev seas, particularly during June, July, and August.
- Some of the most significant increases in chlorophyll-a concentrations over the years 2003-2017 have occurred during May in localized areas of the Labrador Sea and the Barents Sea.
Autotrophic minute algae living in the sea ice (ice algae) and water column (phytoplankton) are the main primary producers in the Arctic Ocean. Through photosynthesis, they transform dissolved inorganic carbon dioxide into organic material. Consequently, primary production provides a key ecosystem service by providing energy to the entire food web in the oceans. The global oceans play a significant role in global carbon budgets via photosynthesis, contributing approximately half of Earth’s net annual photosynthesis with ~10-15% of this production occurring on the continental shelves alone (Müller-Karger et al., 2005). Primary productivity is strongly dependent upon light availability and the presence of nutrients, and thus is highly seasonal in the Arctic region. In particular, the melting and retreat of sea ice during spring are strong drivers of primary production in the Arctic Ocean and its adjacent shelf seas due to enhanced light availability and stratification (Barber et al., 2015; Leu et al., 2015; Ardyna et al., 2017). Recent declines in Arctic sea ice extent (see the essay on Sea Ice) have contributed substantially to shifts in primary productivity throughout the Arctic Ocean. However, the response of primary production to sea ice loss has been both seasonally and spatially variable (e.g., Tremblay et al., 2015; Hill et al., 2017).
Here we present satellite-based estimates of algal chlorophyll-a (occurring in all species of phytoplankton), based on the color of the ocean, and subsequently provide calculated primary production estimates. These results are shown for ocean areas with less than 15% sea ice concentration and, therefore, do not include production by sea ice algae, open water from within the sea ice pack, or under-ice phytoplankton blooms.
Measurements of the algal pigment chlorophyll (e.g., chlorophyll-a) serve as a proxy for the amount of algal biomass present as well as overall plant health. Here we present the complete, updated MODIS-Aqua satellite chlorophyll-a record for the northern polar region for the years 2003-2017. A base period of 2003-2016 is chosen to calculate the 2017 anomalies to maximize the length of the short satellite-based time series.
The 2017 data show a distribution of both positive and negative anomalies in chlorophyll-a concentrations in a number of locations across the Arctic Ocean region, where patterns are spatially and temporally heterogeneous (Fig. 1). These patterns are often associated with the timing of sea ice breakup: positive anomalies tend to occur in regions where the breakup is relatively early, while negative anomalies tend to occur in regions where the breakup is delayed. The most notable positive anomaly in 2017 occurred during May, with high concentrations of chlorophyll-a (averaging over ~12 mg m-3 higher than the 2003-2016 mean) occurring across a relatively large (~500 x 350 km) region in the northwestern Bering Sea (Figs. 1a and 1e). Strong positive anomalies in chlorophyll-a during May also occurred in the southeastern Chukchi Sea (off the coast of Point Hope, Alaska), where values averaged ~16 mg m-3 higher than the 2003-2016 mean across a ~100 x 150 km area (Figs. 1a and 1e). One additional positive anomaly of note occurred in the northern Barents Sea (west of Novaya Zemlya) during June (Fig. 1f), where 2017 values were ~8 mg m-3 higher than the 2003-2016 mean. These positive anomalies are in contrast to widespread negative chlorophyll anomalies across the Barents Sea in May (Fig. 1e). Other widespread negative anomalies occurred across Baffin Bay during May (Fig. 1e) and the Kara and Laptev seas during all months (Figs. 1e, 1f, 1g and 1h).
The most significant rates of change in the 2003-2017 satellite record in May have occurred southwest of Greenland in the Labrador Sea and to the west of Novaya Zemlya in the Barents Sea (Fig. 2a) and reflect increasing chlorophyll-a concentrations. The increase in the Barents Sea has been associated with declines in sea ice (Fig. 1i) linked to the Atlantic Water inflow (e.g., Alexeev et al., 2013). Positive trends are less pronounced but become increasingly widespread here during June, July and August (Fig. 2b, 2c and 2d).
To illustrate the quantitative nature of these trends, three example “hotspot” regions (shown in Fig. 1i) with notably steep trends in chlorophyll-a for May, June, July and August 2003-2017 are shown in Fig. 3. Statistically significant trends (p < 0.1) occur in the region in the Laptev Sea (A), northwest of the New Siberian Islands, during June (Fig. 3a); during all months (May, June, July and August) in the region in the Barents Sea (B), west of Novaya Zemlya (Fig. 3b); and during May in the region in the Labrador Sea (C), southwest of Greenland (Fig. 3c). The largest blooms take place in May for the Barents and Labrador sea sites, but are delayed until August for the Laptev Sea site owing to the later breakup of sea ice across that region. The largest increases in chlorophyll-a concentrations have occurred during May in the Labrador Sea (Fig. 3c) and the Barents Sea (Fig. 3b). In May 2017, there were relatively low chlorophyll-a concentrations at the Barents Sea site followed by relatively high concentrations in June (Fig. 3b). While many of these patterns are directly linked to sea ice variability (and therefore light availability), it is important to note that there are other dominant factors at play that add to the complexity of observed chlorophyll-a concentrations, such as the distribution and availability of nutrients.
Chlorophyll-a concentrations give an estimate of the standing stock of algal biomass. Rates of primary production (i.e., the production of carbon via photosynthesis) give a slightly different perspective, and are calculated by combining chlorophyll-a concentrations with sea surface temperatures, incident solar irradiance, and mixed layer depths. Estimates of ocean primary productivity for nine regions (and the average of these nine regions) across the Arctic, relative to the 2003-2016 base period, indicate above average primary productivity for 2017 in all regions (Fig. 4, Table 1). Areas with the highest anomalies for 2017 include the Hudson Bay and Amerasian Arctic regions. In the longer term, positive trends in primary productivity occurred in all regions during the period 2003-2017 (Fig. 4, Table 1). Statistically significant trends occurred in the Eurasian Arctic, Barents Sea, Greenland Sea, Hudson Bay and North Atlantic, with the steepest trends found for the Barents Sea (15.9 g C/m2/yr/dec) and the Eurasian Arctic (14.4 g C/m2/yr/dec).
|% Change||2017 Anomaly
from a 2003-2016 base period
from a 2003-2016 base period
|Sea of Okhotsk||4.06||0.282||8.1||2.14||2.9|
|Baffin Bay/Labrador Sea||6.32||0.093||16.8||6.13||10.8|
|Average of Nine Regions||7.55||0.000||19.4||4.92||8.3|
While similar trends have been reported previously for these regions using both SeaWiFS and MODIS data (Comiso, 2015), satellite evidence does suggest that recent increases in cloudiness have dampened the increases in production that would have otherwise occurred as a function of sea ice decline alone (Bélanger et al., 2013). Further challenges remain with linking primary productivity, as well depth-integrated chlorophyll biomass throughout the water column, to satellite-based surface chlorophyll-a values (Babin et al., 2015; Lee et al., 2015; Tremblay et al., 2015; Kahru, 2017). Satellite-based chlorophyll-a and primary productivity estimates continue to be confounded by issues such as river turbidity in coastal regions (e.g., Demidov et al., 2014; Chaves et al., 2015) and the presence of sea ice. Efforts to improve satellite retrieval algorithms based on in situ observations are thus critical to continue in all regions of the Arctic.
Alexeev, V. A., V. V. Ivanov, R. Kwok, and L. H. Smedsrud, 2013: North Atlantic warming and declining volume of arctic sea ice. The Cryosphere Discuss., 7, 245-265, doi: 10.5194/tcd-7-245-2013.
Ardyna, M., M. Babin, E. Devred, A. Forest, M. Gosselin, P. Raimbault, and J. -É. Tremblay, 2017: Shelf-basin gradients shape ecological phytoplankton niches and community composition in the coastal Arctic Ocean (Beaufort Sea). Limnology and Oceanography, 62, 2113-2132, doi: 10.1002/lno.10554.
Babin, M., S. Bélanger, I. Ellinsten, A. Forest, V. Le Fouest, T. Lacour, M. Ardyna, and D. Slagstad, 2015: Estimation of primary production in the Arctic Ocean using ocean colour remote sensing and coupled physical-biological models: Strengths, limitations and how they compare. Progress in Oceanography, 139, 197-220, doi: 10.1016/j.pocean.2015.08.008.
Barber, D. G., H. Hop, C. J. Mundy, B. Else, I. A. Dmitrenko, J. -É. Tremblay, J. K. Ehn, P. Assmy, M. Daase, L. M. Candlish, and S. Rysgaard, 2015: Selected physical, biological and biogeochemical implications of a rapidly changing Arctic Marginal Ice Zone. Progress in Oceanography, 139, 122-150, doi: 10.1016/j.pocean.2015.09.003.
Behrenfeld, M. J., and P. G. Falkowski, 1997: Photosynthetic rates derived from satellite-based chlorophyll concentration. Limnology and Oceanography, 42(1), 1-20.
Bélanger, S., M. Babin, and J. -É. Tremblay, 2013: Increasing cloudiness in Arctic damps the increase in phytoplankton primary production due to sea ice receding. Biogeosciences, 10, 4087-4101, doi: 10.5194/bg-10-4087-2013.
Cavalieri, D. J., C. L. Parkinson, P. Gloersen, and H. Zwally, 1996, updated yearly: Sea Ice Concentrations from Nimbus-7 SMMR and DMSP SSM/I-SSMIS Passive Microwave Data. [2003-2014]. Boulder, Colorado, USA: NASA DAAC at the National Snow and Ice Data Center.
Chaves, J., P. J. Werdell, C. W. Proctor, A. R. Neeley, S. A. Freeman, C. S. Thomas, and S. B. Hooker, 2015: Assessment of ocean color data records from MODIS-Aqua in the western Arctic Ocean. Deep-Sea Research II-Part A, 118, 32-43, doi: 10.1016/j.dsr2.2015.02.011.
Comiso, J. C., 2015: Variability and trends of the global sea ice covers and sea levels: Effects on physicochemical parameters in Climate and Fresh Water Toxins, L. M. Botana, M. C. Lauzao, and N. Vilarino, Eds., De Gruyter, Berlin, Germany.
Demidov, A. B., S. A. Mosharov, and P. N. Makkaveev, 2014: Patterns of the Kara Sea primary production in autumn: Biotic and abiotic forcing of subsurface layer. Journal of Marine Systems, 132, 130-149, doi: 10.1016/j.jmarsys.2014.01.014.
Hill, V., M. Ardyna, S. H. Lee, and D. E. Varela, 2017: Decadal trends in phytoplankton production in the Pacific Arctic Region from 1950 to 2012. Deep-Sea Research Part II, http://dx.doi.org/10.1016/j.dsr2.2016.12.015.
Kahru, M., 2017: Ocean productivity from space: Commentary. Global Biogeochem. Cycles, 31, 214-216, doi: 10.1002/2016GB005582.
Lee, Y. J., et al., 2015: An assessment of phytoplankton primary productivity in the Arctic Ocean from satellite ocean color/in situ chlorophyll-a based models. Journal of Geophysical Research-Oceans, 120, 6508-6541, doi: 10.1002/2015JC011018.
Leu, E., C. J. Mundy, P. Assmy, K. Campbell, T. M. Gabrielsen, M. Gosselin, T. Juul-Pedersen, and R. Gradinger, 2015: Arctic spring awakening – Steering principles behind the phenology of vernal ice algal blooms. Progress in Oceanography, 139, 151-170, http://dx.doi.org/10.1016/j.pocean.2015.07.012.
Maslanik, J., and J. Stroeve, 1999, updated daily: Near-Real-Time DMSP SSM/I-SSMIS Daily Polar Gridded Sea Ice Concentrations. . Boulder, Colorado, USA: NASA DAAC at the National Snow and Ice Data Center.
Müller-Karger, F. E., R. Varela, R. Thunell, R. Luerssen, C. Hu, and J. J. Walsh, 2005: The importance of continental margins in the global carbon cycle. Geophysical Research Letters, 32, L01602, doi: 10.1029/2004GL021346.
Tremblay, J. -É., L. G. Anderson, P. Matrai, S. Bélanger, C. Michel, P. Coupel, and M. Reigstad, 2015: Global and regional drivers of nutrient supply, primary production and CO2 drawdown in the changing Arctic Ocean. Progress in Oceanography, 139, 171-196, doi: 10.1016/j.pocean.2015.08.009.
November 30, 2017