Christopher L. Follett
Massachusetts Institute of Technology
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Featured researches published by Christopher L. Follett.
Proceedings of the National Academy of Sciences of the United States of America | 2014
Christopher L. Follett; Daniel J. Repeta; Daniel H. Rothman; Li Xu; Chiara Santinelli
Significance Oceanic dissolved organic carbon (DOC) contains as much carbon as Earth’s atmosphere, yet its cycling timescales and composition remain poorly constrained. We use serial oxidation experiments to measure the quantitative distribution of carbon isotopes inside the DOC reservoir, allowing us to estimate both its cycling timescales and source distribution. We find that a large portion of deep water DOC has a modern radiocarbon age and a fast turnover time supported by particle dissolution. In addition, stable carbon isotopes allow for diverse sources of carbon, besides microbial production, to quantitatively feed this reservoir. Our work suggests a DOC cycle that is far more intricate, and potentially variable on shorter timescales, than previously envisioned. Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ13C and age via Δ14C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle.
Global Biogeochemical Cycles | 2018
B. B. Cael; Kelsey Bisson; Christopher L. Follett
We describe the basis of a theory for interpreting measurements of two key biogeochemical fluxes—primary production by phytoplankton (p, μg C · L−1 · day−1) and biological carbon export from the surface ocean by sinking particles (f, mg C · m−2 · day−1)—in terms of their probability distributions. Given that p and f are mechanistically linked but variable and effectively measured on different scales, we hypothesize that a quantitative relationship emerges between collections of the two measurements. Motivated by the many subprocesses driving production and export, we take as a null model that large‐scale distributions of p and f are lognormal. We then show that compilations of p and f measurements are consistent with this hypothesis. The compilation of p measurements is extensive enough to subregion by biome, basin, depth, or season; these subsets are also well described by lognormals, whose log‐moments sort predictably. Informed by the lognormality of both p and f we infer a statistical scaling relationship between the two quantities and derive a linear relationship between the log‐moments of their distributions. We find agreement between two independent estimates of the slope and intercept of this line and show that the distribution of f measurements is consistent with predictions made from the moments of the p distribution. These results illustrate the utility of a distributional approach to biogeochemical fluxes. We close by describing potential uses and challenges for the further development of such an approach.
Marine Chemistry | 2015
Chiara Santinelli; Christopher L. Follett; Simona Retelletti Brogi; Li Xu; Daniel J. Repeta
The ISME Journal | 2018
Christopher L. Follett; Stephanie Dutkiewicz; David M. Karl; Keisuke Inomura; Michael J. Follows
Limnology and Oceanography | 2018
Christopher L. Follett; Angelicque E. White; Samuel T. Wilson; Michael J. Follows
Global Biogeochemical Cycles | 2018
B. B. Cael; Kelsey Bisson; Christopher L. Follett
Frontiers | 2018
Michael C. G. Carlson; B. B. Cael; Christopher L. Follett; Michael J. Follows
Atmospheric Measurement Techniques Discussions | 2018
Rachel E. O apos; Brien; Kelsey J. Ridley; Manjula R. Canagaratna; John T. Jayne; Philip Croteau; Douglas R. Worsnop; Sri Hapsari Budisulistiorini; Jason D. Surratt; Christopher L. Follett; Daniel J. Repeta; Jesse H. Kroll
Frontiers Research Foundation | 2014
Jamie William Becker; Paul M. Berube; Christopher L. Follett; John B. Waterbury; Sallie W. Chisholm; Edward F. DeLong; Daniel J. Repeta
Archive | 2011
Daniel H. Rothman; Christopher L. Follett