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Evidence for changes in carbon isotopic fractionation by phytoplankton between 1960 and 2010
Author(s) -
Young J. N.,
Bruggeman J.,
Rickaby R. E. M.,
Erez J.,
Conte M.
Publication year - 2013
Publication title -
global biogeochemical cycles
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.512
H-Index - 187
eISSN - 1944-9224
pISSN - 0886-6236
DOI - 10.1002/gbc.20045
Subject(s) - phytoplankton , isotopes of carbon , carbon fibers , fractionation , environmental science , total inorganic carbon , carbon cycle , sediment trap , oceanography , environmental chemistry , dissolved organic carbon , total organic carbon , nutrient , atmospheric sciences , chemistry , geology , ecology , carbon dioxide , biology , ecosystem , materials science , organic chemistry , composite number , composite material
Rising CO 2 is expected to drive a myriad of environmental changes in the surface ocean. Deciphering the phytoplankton response to this complex change is difficult. Here we determine whether a trend in the biological fractionation of stable carbon isotopes ( ε p ) has occurred over the past 50 years. ε p is primarily controlled by the acquisition and intracellular transport of inorganic carbon and the rate of carbon fixation. In turn, these processes are sensitive to phytoplankton physiology, community composition, and notably inorganic carbon availability. ε p may therefore carry a signal of biological response to climate change. Temporal and spatial records of ε p can be deciphered from the difference between the stable carbon isotopic composition of particulate organic matter (δ 13 C POC ) and that of the ambient inorganic carbon pool (δ 13 C CO2 ). Here we establish a global record of ε p extending from the 1960s to today, extracted from a newly compiled data set of global measured δ 13 C POC and part measured/part climatology δ 13 C CO2 . We find that ε p has changed significantly since the 1960s in the low‐ to mid‐latitude surface ocean. The increase is most pronounced in the subtropics, where it is estimated at > 0.015‰ per year. Our findings of such rates of change are further supported by a high resolution temporal record from a single sediment trap near Bermuda. Our results are consistent with the idea that ε p is affected by increased inorganic carbon availability driven by the rise in atmospheric CO 2 .