Rr. Bidigare et al., CONSISTENT FRACTIONATION OF C-13 IN NATURE AND IN THE LABORATORY - GROWTH-RATE EFFECTS IN SOME HAPTOPHYTE ALGAE, Global biogeochemical cycles, 11(2), 1997, pp. 279-292
The carbon isotopic fractionation accompanying formation of biomass by
alkenone-producing algae in natural marine environments varies system
atically with the concentration of dissolved phosphate. Specifically,
if the fractionation is expressed by epsilon(p) approximate to delta(e
) - delta(p), where delta(e) and delta(p) are the delta(13)C values fo
r dissolved CO2 and for algal biomass (determined by isotopic analysts
of C-37 alkadienones), respectively, and if C-e is the concentration
of dissolved CO2, mu mol kg(-1), then b = 38 + 160[PO4], where [PO4]
is the concentration of dissolved phosphate, mu M, and b = (25 - epsil
on(p))C-e. The correlation found between b and [PO4] is due to effects
linking nutrient levels to growth rates and cellular carbon budgets f
or alkenone-containing algae, most likely by trace-metal limitations o
n algal growth. The relationship reported here is characteristic of 39
samples (r(2) = 0.95) from the Santa Monica Basin (six different time
s during the annual cycle), the equatorial Pacific (boreal spring and
fail cruises as well as during an iron-enrichment experiment), and the
Peru upwelling zone. Points representative of samples from the Sargas
so Sea ([PO4] less than or equal to 0.1 mu M) fall above the b = f[PO4
] line. Analysis of correlations expected between mu (growth rate), ep
silon(p), and C-e shows that, for our entire data set, most variations
in epsilon(p) result from variations in mu rather than C-e. According
ly, before concentrations of dissolved CO2 can be estimated from isoto
pic fractionations, some means of accounting for variations in growth
rate must be found, perhaps by drawing on relationships between [PO4]
and Cd/Ca ratios in shells of planktonic foraminifera.