Abstract

We performed a transplant experiment in eutrophic Sau reservoir to assess the factors that control bacterial abundance, activity, growth rate, and community composition. Samples from the lacustrine and the riverine ends of the reservoir were incubated in dialysis bags placed in situ and transplanted to the other side of the reservoir and also incubated after 1 µm filtration to measure predator effects. The bags were sampled at 12‐h intervals to estimate bacterial abundance, whole community activity, activity structure (by flow cytometry), and phylogenetic composition (by in situ hybridization with group‐specific phylogenetic probes). Bacterial production was always regulated by nutrient supply, but abundance and activity were differently regulated at both sites. The riverine bacteria were limited by predator activity, whereas the lacustrine were regulated by a combination of predation and nutrient supply. Therefore, even in the same environment, different modes of control can act simultaneously. Bacterial activity structure was also regulated in the same way. Abundance of high DNA bacteria and cells hybridizing with the universal EUB338 probe were well correlated. In the lacustrine sample, bacterial community structure did not change significantly, whereas in the riverine sample, Α‐ and Δ‐Proteobacteria reduced their growth when transplanted, whereas Β‐Proteobacteria were stimulated by the presence of predators. Members of the Cytophaga/Flavobacterium phylum grew only when incubated in situ in the absence of predators. This different behavior in the different bacterial groups resulted in strong changes in bacterial assemblage composition, evident already after 24 h. The experiment demonstrates that, together with the effect of predators, nutrient supply affects bacterial community properties and that a complex regulation involving both types of control can occur in a single heterogeneous planktonic system.

Highlights

  • We performed a transplant experiment in eutrophic Sau reservoir to assess the factors that control bacterial abundance, activity, growth rate, and community composition

  • Even though bacteria were more concentrated (Fig. 2) in the river side (ϳ1.2 107 ml Ϫ1) than in the Dam side (ϳ4 106 ml Ϫ1), a clear decrease in bacterial abundance occurred as soon as the river entered the lacustrine part of the reservoir; bacterial abundance at 14 km from the Dam was already slightly lower than that at the Dam site

  • More conspicuous than the changes in bacterial abundance were the changes in the relative proportion of HighDNA and LowDNA bacteria, such that the river sample was composed of HighDNA bacteria up to 90% of total bacterial abundance whereas LowDNA bacteria dominated in the lacustrine part of the reservoir (%HDNA ϭ 30)

Read more

Summary

Introduction

We performed a transplant experiment in eutrophic Sau reservoir to assess the factors that control bacterial abundance, activity, growth rate, and community composition. The bags were sampled at 12-h intervals to estimate bacterial abundance, whole community activity, activity structure (by flow cytometry), and phylogenetic composition (by in situ hybridization with group-specific phylogenetic probes). The riverine bacteria were limited by predator activity, whereas the lacustrine were regulated by a combination of predation and nutrient supply. Members of the Cytophaga/Flavobacterium phylum grew only when incubated in situ in the absence of predators This different behavior in the different bacterial groups resulted in strong changes in bacterial assemblage composition, evident already after 24 h. The experiment demonstrates that, together with the effect of predators, nutrient supply affects bacterial community properties and that a complex regulation involving both types of control can occur in a single heterogeneous planktonic system. Bacteria are relevant members of the limnetic planktonic food web, both in terms of biomass and production share (e.g., Cole and Caraco 1993; del Giorgio and Gasol 1995) and while this is very evident in oligotrophic plankton sys-

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.