Rw. Sanders et al., Heterotrophic and mixotrophic nanoplankton predation on picoplankton in the Sargasso Sea and on Georges Bank, MAR ECOL-PR, 192, 2000, pp. 103-118
Nanoplankton and picoplankton abundance and community grazing on picoplankt
on were determined in summer and autumn at several stations in a productive
coastal environment (Georges Bank, NW Atlantic Ocean) and in an oligotroph
ic oceanic ecosystem (Sargasso Sea). Ranges of heterotrophic nanoplankton (
HNAN) abundance were 1.2 to 3.6 x 10(3) cells ml(-1) on Georges Bank, and 2
.2 to 6.8 x 10(2) cells ml(-1) in the Sargasso Sea. Ranges of phototrophic
nanoplankton (PNAN) abundance in these ecosystems were 1.9 to 6.0 x 10(3) a
nd 1.3 to 4.7 x 10(2), respectively. Mixotrophic nanoplankton (MNAN), opera
tionally defined here as chloroplast-bearing nanoplankton that ingested flu
orescent tracers, comprised an average of 12 to 17% of PNAN in surface wate
rs in both environments during August and October. Mixotrophs at specific s
tations constituted as much as 38% of total PNAN abundance on Georges Bank
and 30% in the Sargasso Sea. Mixotrophs represented up to 39% of the total
phagotrophic nanoplankton abundance (MNAN/[MNAN + HNAN]). Community grazing
impact was estimated from the disappearance of fluorescent prey surrogates
(fluorescently labeled bacteria, FLB; cyanobacteria, FLC; and <3 mu m alga
e, FLA). Absolute grazing rates (total picoplankton cells removed d(-1)) on
Georges Bank exceeded those in the Sargasso Sea due to the greater abundan
ces of predators and prey. However, there was overlap in the specific grazi
ng losses at the 2 sites (ranges = 0.08 to 0.38 d(-1) in the coastal ocean
and 0.05 to 0.24 d(-1) in the oligotrophic ocean). Rates of bacterivory wer
e in approximate balance with rates of bacterial production (H-3-thymidine
uptake), but production exceeded bacterivory on Georges Bank during the sum
mer cruise. These data are among the first documenting the impact of grazin
g on picoplankton in these environments, and they are consistent with the p
rediction that nanoplanktonic protists are major predators of picoplankton.
While the proportion of phototrophs that are phagotrophic was highly varia
ble, our study indicates that algal mixotrophy is widespread in the marine
environment, occurring in both coastal and oligotrophic sites, and should b
e considered quantitatively in microbial food web investigations.