Our oceans account for the
biggest CO2 storage on the planet, trough the accumulation by phytoplankton.
This carbon is further accumulated by zooplankton or other heterotrofic
microbes. Eventually, about 10% is exported to sediments in the deep ocean and
90% is recirculated in the so-called biological carbon pump. This mechanism is
regulated by microbiological processes, but it is yet unclear how these biotic
interactions are involved. Guidi et al. (2016) analysed the entire planktonic
ecosystem in order to capture it’s internal structure with regards to the
biological carbon pump and the biogeochemical and abiotic aspects involved.
Using data from The Tara
Oceans expedition, Guidi et al. (2016) assessed the carbon export at 150 m,
coupled with the ecosystem structure and its functional repertoire. Plankton
samples and environmental data were gained crossing diverse oceans. These
global-scale genomic data-sets from the euphotic zone and the associated
(a)biotic parameters were combined and used for regression based modelling.
This resulted in the reveal of of some high correlations between the relative sequence
abundance of several plankton lineages and environmental parameters, like
carbon export and NPP. However, these links between lineages and environmental
parameters still doesn’t show the intrinsic structure of the biological carbon
pump. Therefore, in the second part of this study (Guide et al., 2016) it was
attempted to set up a network of lineages and gene functions with the links
expressed in robustness of the co-occurence between them. This network was then
clustered into subnetworks, in order to find significant traits that relate
specifically to this subnetwork. Analyzing these subnetwork-trait relationships,
emphasized the key nodes in each subnetwork, which made it possible to
summarize the microbial communities (or subnetworks) related to carbon export
in the euphotic zone of the oceans.
This method was applied to
data sets for eukaryotes, prokaryotes and viruses found in the planktonic
samples form The Tara Oceans expedition. Within each dataset, different
subnetworks have been identified related to the carbon export. For example, 20%
of the eukaryotic lineages were photosynthetic organisms. Although this forms a
small subnetwork, it’s structure unsurprisingly showed to have a strong
correlation with carbon export. Also, 69% of the carbon export variability at
150 m can be explained by this subnetwork. The prokaryotic subnetwork that was
most related to carbon export, contained 109 OTU’s (operational taxonomic
unit), that is: 109 groups of closely related prokaryotes. The most significant
organism in this community was Synechococcus.
Strikingly, two phages of this prokaryote function as key elements in the viral
subnetwork strongest correlated to the carbon export (r=0.93). These findings
may seem conflicting, but they actually indicate two sided stimulation of the carbon export. That is, there are hints that the phages increase the carbon export intensity by producing colloidal particles and forming aggregates (Suttle, 2007) rather than decreasing the intensity by the viral lysis of Synochoccus (Weinbauer, 2004).
Finally, these different
subnetworks were integretated with the use of a more general co-occurence
network that was established earlier (Lima-Mendez, G. et al., 2015). An
important feature of this ecological structure visualisation is the mutual
exclusivity between two hub lineages. The same analytical methods used in this
research are used to study prokaryotic functions (in other words, orthologous
groups of genes) as well. This resulted in another co-occurrence network for
functions that occur in the euphotic zone. Two subnetworks can be distinguished
by functions related to relatively photosynthesis and growth, and formation and
degradation of marine aggregates.
Although studies carried
out in the past decades focused on finding key players in the carbon accumulating
and circulating mechanism (Sancetta et al., 1991; Scharek et al,. 1999; Richardson et al., 2007; Turner, 2015), the use of environmental and metagenomic data to get
more insight into the biological carbon pump is a new approach to this issue. The
resulting network highlights the potential of certain lineages as strategic key
roles, especially of some lineages which value in this context was
under-appreciated. Therefore we have now even more food for thought, be it more
structured and clearer by the ecological context in which it is now placed. Also, further examination of ecological processes within the biological carbon pump may be of big importance to climate change research, since phytoplankton and oceanic carbon sinks play a significant role in this.
Article reviewed:
Guidi, L., Chaffron, S.,
Bittner, L., Eveillard, D., Larhlimi, A., Roux, S., ... & Coelho, L. P.
(2016). Plankton networks driving carbon export in the oligotrophic ocean. Nature.
References:
- Lima-Mendez, G., Faust, K., Henry, N., Decelle, J., Colin, S., Carcillo, F., ... & Bittner, L. (2015). Determinants of community structure in the global plankton interactome. Science, 348(6237), 1262073.
- Richardson, T. L., & Jackson, G. A. (2007). Small phytoplankton and carbon export from the surface ocean. Science, 315(5813), 838-840.
- Sancetta, C., Villareal, T., & Falkowski, P. (1991). Massive fluxes of rhizosolenid diatoms: a common occurrence?. Limnology and Oceanography,36(7), 1452-1457.
- Scharek, R., Tupas, L. M., & Karl, D. M. (1999). Diatom fluxes to the deep sea in the oligotrophic North Pacific gyre at Station ALOHA. Marine Ecology Progress Series, 182, 55-67.
- Suttle, C. A. (2007). Marine viruses—major players in the global ecosystem.Nature Reviews Microbiology, 5(10), 801-812.
- Weinbauer, M. G. (2004). Ecology of prokaryotic viruses. FEMS microbiology reviews, 28(2), 127-181.
- Lima-Mendez, G., Faust, K., Henry, N., Decelle, J., Colin, S., Carcillo, F., ... & Bittner, L. (2015). Determinants of community structure in the global plankton interactome. Science, 348(6237), 1262073.
- Richardson, T. L., & Jackson, G. A. (2007). Small phytoplankton and carbon export from the surface ocean. Science, 315(5813), 838-840.
- Sancetta, C., Villareal, T., & Falkowski, P. (1991). Massive fluxes of rhizosolenid diatoms: a common occurrence?. Limnology and Oceanography,36(7), 1452-1457.
- Scharek, R., Tupas, L. M., & Karl, D. M. (1999). Diatom fluxes to the deep sea in the oligotrophic North Pacific gyre at Station ALOHA. Marine Ecology Progress Series, 182, 55-67.
- Suttle, C. A. (2007). Marine viruses—major players in the global ecosystem.Nature Reviews Microbiology, 5(10), 801-812.
- Weinbauer, M. G. (2004). Ecology of prokaryotic viruses. FEMS microbiology reviews, 28(2), 127-181.
Hi Thyrza,
ReplyDeletethanks for your review!
We heard about the important role of Synechococcus and also Prochlorococcus for oxygen production before. So I thought that both should also be important organisms for the carbon fixation. You wrote that 'The most significant organism in this community was Synechococcus.'. Did the study mention Prochlorococcus in regard to the carbon fixation or was I wrong with my suggestion Prochlorococcus being as important as Synechococcus for carbon fixation?
Thanks,
Eleni