The Cyanobacteria Prochlorococcus and Synechococcus account for a substantial fraction of marine primary production. Here, we present quantitative niche models for these lineages that assess present and future global abundances and distributions. These niche models are the result of neural network, nonparametric, and parametric analyses, and they rely on >35,000 discrete observations from all major ocean regions. The models assess cell abundance based on temperature and photosynthetically active radiation, but the individual responses to these environmental variables differ for each lineage. The models estimate global biogeographic patterns and seasonal variability of cell abundance, with maxima in the warm oligotrophic gyres of the Indian and the western Pacific Oceans and minima at higher latitudes. The annual mean global abundances of Prochlorococcus and Synechococcus are 2.9 ± 0.1 × 10 27 and 7.0 ± 0.3 × 10 26 cells, respectively. Using projections of sea surface temperature as a result of increased concentration of greenhouse gases at the end of the 21st century, our niche models projected increases in cell numbers of 29% and 14% for Prochlorococcus and Synechococcus, respectively. The changes are geographically uneven but include an increase in area. Thus, our global niche models suggest that oceanic microbial communities will experience complex changes as a result of projected future climate conditions. Because of the high abundances and contributions to primary production of Prochlorococcus and Synechococcus, these changes may have large impacts on ocean ecosystems and biogeochemical cycles.climate change | marine biogeochemistry | microbial biogeography M arine phytoplankton contribute roughly one-half of the global net primary production and play a key role in regulating global biogeochemical cycles (1). Marine phytoplankton are very diverse (2), including phylogenetic, biochemical, metabolic, and ecological variability (3-6). Thus, understanding the contribution of different phytoplankton groups to ecosystem functioning is central to predicting the biogeochemical impact of future environmental changes (7). However, our limited quantitative understanding of the global distribution and abundance of most phytoplankton groups constrains our ability to incorporate phytoplankton diversity into ocean biogeochemical models.The marine Cyanobacteria Prochlorococcus and Synechococcus are abundant in many ocean regions. The known geographical distributions of the two lineages are based primarily on individual cruises or time series observations and secondarily on macroecological descriptions, indicating central tendencies and boundary constraints related to light, temperature, nutrients, and chlorophyll a concentration (8-10). Prochlorococcus is present from the surface to a depth of ∼150 m in the open ocean between 40°N and 40°S. The population size declines beyond these latitudinal limits, and Prochlorococcus is thought to be absent at temperatures below 15°C (11). Furthermore, the lineage is believed to be out...
As climate changes and the upper Arctic Ocean receives more heat and fresh water, it becomes more difficult for mixing processes to deliver nutrients from depth to the surface for phytoplankton growth. Competitive advantage will presumably accrue to small cells because they are more effective in acquiring nutrients and less susceptible to gravitational settling than large cells. Since 2004, we have discerned an increase in the smallest algae and bacteria along with a concomitant decrease in somewhat larger algae. If this trend toward a community of smaller cells is sustained, it may lead to reduced biological production at higher trophic levels.
A partitioning of ultraphytoplankton primary production among prochlorophytes, cyanobacteria, and eucaryotic algae was made by shipboard flow cytometric sorting of 10C‐labeled cells. Aggregate primary production was derived from the sum, over all three ultraplankton groups, of the product of cell abundance and cell‐specific rate of 14C uptake which ranged from 0.03 to 4 fg C cell−1 h−1 for prochlorophytes and 0.2 to 10 fg C cell−1 h−1 for cyanobacteria. Results indicated that the dominant primary producer was not necessarily the numerical dominant nor necessarily the group with the highest cell‐specific rate of 14C uptake. Generally, eucaryotic ultraphytoplankton are dominant because of their high cell‐specific rate of 14C uptake and in spite of their relatively low abundance. Less often, it seems, procaryotic picoplankton may dominate in spite of their low cell‐specific rate of 14C uptake because of their high abundance.
The macroecological relationships among marine phytoplankton total cell density, community size structure and temperature have lacked a theoretical explanation. The tiniest members of this planktonic group comprise cyanobacteria and eukaryotic algae smaller than 2 lm in diameter, collectively known as picophytoplankton. We combine here two ecological rules, the temperature-size relationship with the allometric sizescaling of population abundance to explain a remarkably consistent pattern of increasing picophytoplankton biomass with temperature over the À0.6 to 22 1C range in a merged dataset obtained in the eastern and western temperate North Atlantic Ocean across a diverse range of environmental conditions. Our results show that temperature alone was able to explain 73% of the variance in the relative contribution of small cells to total phytoplankton biomass regardless of differences in trophic status or inorganic nutrient loading. Our analysis predicts a gradual shift toward smaller primary producers in a warmer ocean. Because the fate of photosynthesized organic carbon largely depends on phytoplankton size, we anticipate future alterations in the functioning of oceanic ecosystems.
Increasing global temperatures are having a profound impact in the Arctic, including the dramatic loss of multiyear sea ice in 2007 that has continued to the present. The majority of life in the Arctic is microbial and the consequences of climate-mediated changes on microbial marine food webs, which are responsible for biogeochemical cycling and support higher trophic levels, are unknown. We examined microbial communities over time by using high-throughput sequencing of microbial DNA collected between 2003 and 2010 from the subsurface chlorophyll maximum (SCM) layer of the Beaufort Sea (Canadian Arctic). We found that overall this layer has freshened and concentrations of nitrate, the limiting nutrient for photosynthetic production in Arctic seas, have decreased. We compared microbial communities from before and after the record September 2007 sea ice minimum and detected significant differences in communities from all three domains of life. In particular, there were significant changes in species composition of Eukarya, with ciliates becoming more common and heterotrophic marine stramenopiles (MASTs) accounting for a smaller proportion of sequences retrieved after 2007. Within the Archaea, Marine Group I Thaumarchaeota, which earlier represented up to 60% of the Archaea sequences in this layer, have declined to <10%. Bacterial communities overall were less diverse after 2007, with a significant decrease of the Bacteroidetes. These significant shifts suggest that the microbial food webs are sensitive to physical oceanographic changes such as those occurring in the Canadian Arctic over the past decade.
By using data collected during a continuous circumnavigation of the Southern Hemisphere, we observed clear patterns in the population-genetic structure of Prochlorococcus, the most abundant photosynthetic organism on Earth, between and within the three Southern Subtropical Gyres. The same mechanisms that were previously invoked to account for the vertical distribution of ecotypes at local scales accounted for the global (horizontal) patterns we observed. Basin-scale and seasonal variations in the structure and strength of vertical stratification provide a basis for understanding large-scale horizontal distribution in genetic and physiological traits of Prochlorococcus, and perhaps of marine microbial communities in general.
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