TL;DR: Evidence is presented to suggest that numbers of free bacteria are controlled by nanoplankton~c heterotrophic flagellates which are ubiquitous in the marine water column, thus providing the means for returning some energy from the 'microbial loop' to the conventional planktonic food chain.
Abstract: Recently developed techniques for estimating bacterial biomass and productivity indicate that bacterial biomass in the sea is related to phytoplankton concentration and that bacteria utilise 10 to 50 % of carbon fixed by photosynthesis. Evidence is presented to suggest that numbers of free bacteria are controlled by nanoplankton~c heterotrophic flagellates which are ubiquitous in the marine water column. The flagellates in turn are preyed upon by microzooplankton. Heterotrophic flagellates and microzooplankton cover the same size range as the phytoplankton, thus providing the means for returning some energy from the 'microbial loop' to the conventional planktonic food chain.
TL;DR: The results support claims in the literature that microbial grazers may perform important regulatory functions at critical times in the growth of plants and support a conceptual model proposed in which microfloral grazers were considered as separate state variables.
Abstract: The most common system responses attributed to microfloral grazers (protozoa, nema- todes, microarthropods) in the literature are increased plant growth, increased N uptake by plants, decreased or increased bacterial populations, increased CO2 evolution, increased N and P mineral- ization, and increased substrate utilization. Based on this evidence in the literature, a conceptual model was proposed in which microfloral grazers were considered as separate state variables. To help evaluate the model, the effects of microbivorous nematodes on microbial growth, nutrient cycling, plant growth, and nutrient uptake were examined with reference to activities within and outside of the rhizosphere. Blue grama grass (Bouteloua gracilis) was grown in gnotobiotic microcosms containing sandy loam soil low in inorganic N, with or without chitin amendments as a source of organic N. The soil was inoculated with bacteria (Pseudomonas paucimobilis or P. stutzeri) or fungus (Fusarium oxysporum), with half the bacterial microcosms inoculated with bacterial-feeding nematodes (Pelodera sp. or Ac- robeloides sp.) and half the fungal microcosms inoculated with fungal-feeding nematodes (Aphelenchus avenae). Similar results were obtained from both the unamended and the chitin-amended experiments. Bacteria, fungi, and both trophic groups of nematodes were more abundant in the rhizosphere than in nonrhizosphere soil. All treatments containing nematodes and bacteria had higher bacterial densities than similar treatments without nematodes. Plants growing in soil with bacteria and bacterial-feeding nematodes grew faster and initially took up more N than plants in soil with only bacteria, because of increased N mineralization by bacteria, NH4+-N excretion by nematodes, and greater initial exploi- tation of soil by plant roots. Addition of fungal-feeding nematodes did not increase plant growth or N uptake because these nematodes excreted less NH4+-N than did bacterial-feeding nematode pop- ulations and because the N mineralized by the fungus alone was sufficient for plant growth. Total shoot P was significantly greater in treatments with fungus or Pelodera sp. than in the sterile plant control or treatments with plants plus Pseudomonas stutzeri until the end of the experiment. The additional mineralization that occurs due to the activities of microbial grazers may be sig- nificant for increasing plant growth only when mineralization by microflora alone is insufficient to meet the plants' requirements. However, while the advantage of increased N mineralization by mi- crobial grazers may be short-term, it may occur in many ecosystems in those short periods of ideal conditions when plant growth can occur. Thus, these results support other claims in the literature that microbial grazers may perform important regulatory functions at critical times in the growth of plants.
TL;DR: Bacterivory in obligate phototrophic algal flagellates may be an important strategy for acquiring nutrients during periods of inorganic nutrient limitation, and Doddema and Van der Veer suggested that phagocytosis might permit utilization of particulate organic N and P when inorganic nutrients are in limited supply.
Abstract: Bacterivory in obligate phototrophic algal flagellates may be an important strategy for acquiring nutrients during periods of inorganic nutrient limitation. Several marine algal flagellates were shown to increase bactivory when phosphate was limited. Grazing on bacteria by algal flagellates was found during blooms of Prymnesium parvum in Sandsljorden, western Norway, in 1989 and Chrysochromulina polylepis on the south and west coast of Norway in 1988. Dissolved phosphate was not detectable in these situations. Algal flagellates may graze bacteria to obtain phosphate, which may permit these algal flagellates to develop blooms when phosphate becomes limited. True mixotrophy, defined as use of particulate organic matter for cellular growth, has been conclusively demonstrated for only a few species in the genus Ochromonas (Fenchel 1982) and for Poteiroochromonas malhamensis (Caron et al. 1990). Much more widespread is the ability to use a restricted range of organic substances, available at high concentrations, as a dietary supplement or sole C source in the dark (Antia 1980). Mixotrophy in algal flagellates has been considered mainly a strategy for gaining C during low light (Bird and Kalff 1987; Sanders and Porter 1988) and therefore has been studied in algae that use bacteria as their primary C source. Doddema and Van der Veer ( 198 3) suggested that phagocytosis might permit utilization of particulate organic N and P when inorganic nutrients are in limited supply. Obligate phototrophs are the appropriate test organisms to evaluate this hypothesis. Bacteria have a high P content even when phosphate is limited (Andersen et al. 1986), although their P content can be reduced when they are drastically starved (Tezuka 1990). Bacteria are therefore a potential source of P when obligate phototrophic algal flagellates are subjected to
TL;DR: Using microfluidics and image analysis of swimming behavior, attraction toward microscale pulses of DMSP and related compounds among several motile strains of phytoplankton, heterotrophic bacteria, and bacterivore and herbivore microzooplankton is observed.
Abstract: Phytoplankton-produced dimethylsulfoniopropionate (DMSP) provides underwater and atmospheric foraging cues for several species of marine invertebrates, fish, birds, and mammals. However, its role in the chemical ecology of marine planktonic microbes is largely unknown, and there is evidence for contradictory functions. By using microfluidics and image analysis of swimming behavior, we observed attraction toward microscale pulses of DMSP and related compounds among several motile strains of phytoplankton, heterotrophic bacteria, and bacterivore and herbivore microzooplankton. Because microbial DMSP cycling is the main natural source of cloud-forming sulfur aerosols, our results highlight how adaptations to microscale chemical seascapes shape planktonic food webs, while potentially influencing climate at the global scale.
TL;DR: Maintenance of adequate soil fertility in systems driven by organic input may require maintenance of food web structure and function as indicated by high levels of enrichment-opportunist bacterivore nematodes, which will require frequent supply of labile organic sources.