The effects of nitrate, ammonium and urea on the growth and colony formation of three strains of Phaeocystis globosa were investigated. Although ammonium and urea supported growth, nitrate was the favoured nitrogen source for the growth of solitary cells for all three strains. Phaeocystis globosa CCMP 1528 and 629 formed colonies in all cultures where nitrate was the sole nitrogen source, but only a few colonies were observed in ammonium and urea treatments. Ammonium and urea were far less effective in supporting growth, biomass generation and colony formation in all three strains. Once colonies developed, colonial cells accounted for at least 15% of the total cells when grown with nitrate; colonial chlorophyll also contributed up to 60% to the total chlorophyll. The growth rates of colonial cells when using nitrate were greater than solitary cells. Changes in colony size, colonial cell abundance and total P. globosa abundance as affected by the nitrogen source may influence the carbon flux within the pelagic food web.

Phaeocystis globosa has become one of the primary causes of harmful algal bloom in coastal areas of southern China in recent years, and it poses a serious threat to the marine environment and other activities depending upon on it (e.g., aquaculture, cooling system of power plants), especially in the Beibu Gulf. We found colonies of P. globosa collected form Guangxi (China) were much larger than those obtained from Shantou cultured in lab. To better understand the causes of giant colonies formation, colonial cells collected from P. globosa GX strain (GX-C) and ST strain (ST-C) were separated by filtration. Morphological observations, phylogenetic analyses, rapid light-response curves, fatty acid profiling and transcriptome analyses of two type cells were performed in the laboratory. Although no differences in morphology and 18S rRNA sequences of these cells were observed, the colonies of GX strain (4.7 mm) are 30 times larger than those produced by the ST strain (300 μm). The rapid light-response curve of GX-C was greater than that of ST-C, consistent with the upregulated photosynthetic system, while the fatty acid content of GX-C was lower than that of ST-C, also consistent with the downregulated synthesis of fatty acids and the upregulated degradation of fatty acids. In summary, the increased energy generated by GX-C is allocated to promote the secretion of extracellular polysaccharides for colony formation. We performed a physiological and molecular assessment of the differences between the GX-C and ST-C strains, providing insights into the mechanisms of giant colonies formation in P. globosa.

Transparent exopolymer particles (TEP) are sticky polymeric substances that are commonly found in the periphery of microbial cells or colonies. They can naturally flocculate smaller suspended particles into larger aggregates and thus play a crucial role in the biological pump and the global carbon cycle. Phytoplankton are the major contributors to marine TEP production, whereas the way TEP production interacts with abiotic factors at the species level is generally unknown but critical for estimating carbon fluxes. In this study, the effects of temperature on TEP production and carbon allocation were studied in two representative diatom species (Nitzschia closterium and Chaetoceros affinis) and two model dinoflagellate species (Prorocentrum micans and Scrippisella trichoidea). The results showed that temperature had a significant impact on TEP production in all species. First, increased temperature promoted the TEP production of all four species. Second, elevated temperature affected the carbon pool allocation, with enhanced dissolved organic carbon (DOC) exudation in the form of TEP in all species. The TEP-C/DOC percentages of N. closterium and P. micans were 93.42 ± 5.88% and 82.03 ± 21.36% at the highest temperature (24 °C), respectively, which was approximately two to five times higher than those percentages at 16 °C. In contrast, TEP’s contribution to the POC pool is lower than that to the DOC pool, ranging from 6.74 ± 0.79% to 28.31 ± 1.79% for all species. Moreover, phytoplankton TEP production may be related to cellular size and physiology. The TEP content produced by the smallest N. closterium (218.96 ± 15.04 fg Xeq./μm³) was ~5 times higher compared to P. micans, S. trichoidea, or C. affinis. In conclusion, TEP production is temperature sensitive and species specific, which should be taken into consideration the regarding TEP-mediated oceanic carbon cycle, particularly in the context of global warming.

Co-culturing and using cell-free filtrates are common methods for investigating allelopathy of marine phytoplankton; however, these methods often yield inconsistent or even contradictory results. The induced release of allelopathic compounds has been hypothesized as a mechanism to explain the discrepancy. Here, we used experiments to assess the inducibility of allelopathy by the diatom, Thalassiosira weissflogii, on the colony formation of Phaeocystis globosa. T. weissflogii and its cell-free filtrates showed inhibitory effects on the growth of solitary P. globosa cells. The colony number, colony diameter, and cells per colony decreased by co-occurring T. weissflogii cells but were enhanced by their extracellular filtrates alone. Living T. weissflogii cells possibly affect the colony integrity by reducing colonial cell density of P. globosa. When P. globosa and T. weissflogii were co-cultured but separated with a 2-µm membrane filter, thus allowing the exchange of extracellular secretions without direct cell contact, P. globosa colony concentration, colony diameter, cells per colony and colonial cell density were inhibited. Once T. weissflogii cells were pre-exposed to cell-free filtrates of P. globosa, their filtrates inhibited colony formation. T. weissflogii had allelopathic effects on P. globosa by releasing extracellular compounds that inhibited growth of solitary cells and colony formation, as well as disrupting colony integrity. However, the allelopathic effects of T. weissflogii on colony formation were only induced when the presence of P. globosa was perceived. Chemically mediated allelopathic effects of diatoms on colony formation of P. globosa may play an important role in the succession of diatoms and Phaeocystis.

Buoyancy Regulation in Phaeocystis globosa Scherffel Colonies