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Appl. Environ. Microbiol., Mar 1996, 986-993, Vol 62, No. 3
JP Montoya, M Voss, P Kahler and DG Capone
We describe a simple, precise, and sensitive experimental protocol for
direct measurement of N(inf2) fixation using the conversion of
(sup15)N(inf2) to organic N. Our protocol greatly reduces the limit of
detection for N(inf2) fixation by taking advantage of the high sensitivity
of a modern, multiple-collector isotope ratio mass spectrometer. This
instrument allowed measurement of N(inf2) fixation by natural assemblages
of plankton in incubations lasting several hours in the presence of
relatively low-level (ca. 10 atom%) tracer additions of (sup15)N(inf2) to
the ambient pool of N(inf2). The sensitivity and precision of this tracer
method are comparable to or better than those associated with the
C(inf2)H(inf2) reduction assay. Data obtained in a series of experiments in
the Gotland Basin of the Baltic Sea showed excellent agreement between
(sup15)N(inf2) tracer and C(inf2)H(inf2) reduction measurements, with the
largest discrepancies between the methods occurring at very low fixation
rates. The ratio of C(inf2)H(inf2) reduced to N(inf2) fixed was 4.68
(plusmn) 0.11 (mean (plusmn) standard error, n = 39). In these experiments,
the rate of C(inf2)H(inf2) reduction was relatively insensitive to assay
volume. Our results, the first for planktonic diazotroph populations of the
Baltic, confirm the validity of the C(inf2)H(inf2) reduction method as a
quantitative measure of N(inf2) fixation in this system. Our (sup15)N(inf2)
protocols are comparable to standard C(inf2)H(inf2) reduction procedures,
which should promote use of direct (sup15)N(inf2) fixation measurements in
other systems.
Copyright © 1996, American Society for Microbiology
A Simple, High-Precision, High-Sensitivity Tracer Assay for N(inf2) Fixation
Biological Laboratories, Harvard University, Cambridge, Massachusetts 02138; Institut fur Ostseeforschung, 18119 Warnemunde, Germany; and Chesapeake Biological Laboratory, Center for Environmental and Estuarine Studies, University of Maryland, Solomons, Maryland 20688-0038
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