COMMUNITY STRUCTURE, PICOPLANKTON GRAZING AND ZOOPLANKTON CONTROL OF HETEROTROPHIC NANOFLAGELLATES IN A EUTROPHIC RESERVOIR DURING THE SUMMER PHYTOPLANKTON MAXIMUM
K. Simek et al., COMMUNITY STRUCTURE, PICOPLANKTON GRAZING AND ZOOPLANKTON CONTROL OF HETEROTROPHIC NANOFLAGELLATES IN A EUTROPHIC RESERVOIR DURING THE SUMMER PHYTOPLANKTON MAXIMUM, Aquatic microbial ecology, 12(1), 1997, pp. 49-63
An intensive 5 wk study was conducted to investigate the role of proti
sts, especially heterotrophic nanoflagellates (HNF), in microbial food
webs during the summer phytoplankton bloom in the epilimnion and meta
limnion of the eutrophic Rimov reservoir (South Bohemia, Czech Republi
c). On average, protists consumed similar to 90% of bacterial producti
on in both layers. The community composition of HNF and the relative i
mportance of different HNF groups as picoplankton consumers were deter
mined. Small HNF (<8 mu m), as chrysomonads, bodonids and choanoflagel
lates, usually accounted for <30% of total HNF biomass but numerically
dominated the community in both layers. They consumed most of (simila
r to 70 to 85 %) the bacterioplankton as well as autotrophic picoplank
ton (APP, exclusively cyanobacteria) production in the reservoir, with
the rest consumed by ciliates. Both ciliates and HNF had higher clear
ance rates on APP than on bacteria and their grazing was likely respon
sible for a sharp decrease in APP abundance (from 3-4 x 10(5) to <2 x
10(3) ml(-1)) and a very constant size structure of bacterioplankton i
n which short rods in the size class of 0.4 to 0.8 mu m constituted 55
to 80 % of the total bacterial biomass in both layers. The proportion
of HNF to total picoplankton biomass in the epilimnion indicated that
the picoplankton biomass was sufficiently high to support HNF growth
for most of the study. Uptake of picoplankton by less numerous, but la
rger, HNF (kathablepharids, Goniomonas sp., and Streptomonas sp.) was
negligible, while their biomass, especially in the metalimnion, exceed
ed that of small HNF and the total biomass of picoplankton. This sugge
sted that food items other than picoplankton were consumed to meet the
ir carbon requirements. Analyzing potential bottom-up and top-down fac
tors controlling HNF numbers and biomass, we did not find a tight rela
tionship between HNF and the concentration of bacteria and chlorophyll
. Variability of HNF abundance and biomass in the epilimnion could lar
gely be explained by cladocerans or by pooled abundances of all potent
ial crustacean consumers of HNF. In the metalimnion, the mean cell vol
ume of HNF was positively linked to chlorophyll but negatively to the
abundance of Cyclopidae and to the pooled abundances of Ceriodaphnia q
uadrangula and Diaphanosoma brachyurum.