Marine Synechococcus picocyanobacteria: Light utilization across latitudes

The most ubiquitous cyanobacteria, Synechococcus, have colonized different marine thermal niches through the evolutionary specialization of lineages adapted to different ranges of temperature seawater. We used the strains of Synechococcus temperature ecotypes to study how light utilization has evolved in the function of temperature. The tropical Synechococcus (clade II) was unable to grow under 16 °C but, at temperatures >25 °C, induced very high growth rates that relied on a strong synthesis of the components of the photosynthetic machinery, leading to a large increase in photosystem cross-section and electron flux. By contrast, the Synechococcus adapted to subpolar habitats (clade I) grew more slowly but was able to cope with temperatures <10 °C. We show that growth at such temperatures was accompanied by a large increase of the photoprotection capacities using the orange carotenoid protein (OCP). Metagenomic analyzes revealed that Synechococcus natural communities show the highest prevalence of the ocp genes in low-temperature niches, whereas most tropical clade II Synechococcus have lost the gene. Moreover, bioinformatic analyzes suggested that the OCP variants of the two cold-adapted Synechococcus clades I and IV have undergone evolutionary convergence through the adaptation of the molecular flexibility. Our study points to an important role of temperature in the evolution of the OCP. We, furthermore, discuss the implications of the different metabolic cost of these physiological strategies on the competitiveness of Synechococcus in a warming ocean. This study can help improve the current hypotheses and models aimed at predicting the changes in ocean carbon fluxes in response to global warming.

Iron Modified Titanate Nanotube Arrays for Photoelectrochemical Removal of E. coli

This study used iron modified titanate nanotube arrays (Fe/TNAs) to remove E. coli in a photoelectrochemical system. The Fe/TNAs was synthesized by the anodization method and followed by the square wave voltammetry electrochemical deposition (SWVE) method with ferric nitrate as the precursor. Fe/TNAs were characterized by SEM, XRD, XPS, and UV-vis DRS to investigate the surface properties and light absorption. As a result, the iron nanoparticles (NPs) were successfully deposited on the tubular structure of the TNAs, which showed the best light utilization. Moreover, the photoelectrochemical (PEC) properties of the Fe/TNAs were measured by current-light response and electrochemical impedance spectroscopy. The photocurrent of the Fe/TNAs-0.5 (3.5 mA/cm2) was higher than TNAs (2.0 mA/cm2) and electron lifetime of Fe/TNAs-0.5 (433.3 ms) were also longer than TNAs (290.3 ms). Compared to the photolytic (P), photocatalytic (PC), and electrochemical (EC) method, Fe/TNAs PEC showed the best removal efficiency for methyl orange degradation. Furthermore, the Fe/TNAs PEC system also performed better removal efficiency than that of photolysis method in E. coli degradation experiments.

Photocatalytic Applications in Wastewater and Air Treatment: A Patent Review (2010–2020)

In this work, we reviewed the most significant patents of the last decade (2010–2020) in the fields of water and air photocatalytic treatment. Patents were discussed by identifying the recurrent addressed issues and presenting the proposed solutions. Adoption of TiO2 and/or modified-TiO2-based material is still the most common choice of inventors, whereas many patents focus on the design of the plants/devices to improve efficiency of photocatalytic treatment by improving light utilization and contact between the phases. The review also highlights issues deriving from specific applications and outlines future trends in the field, such as the need for standardized testing and digitalization of monitoring and control.

Enhanced Photocatalytic Degradation of Perfluorooctanoic Acid by Mesoporous Sb2O3/TiO2 Heterojunctions

Perfluorooctanoic acid (PFOA), a typical perfluorinated carboxylic acid, is an emerging type of permanent organic pollutants that are regulated by the Stockholm Convention. The degradation of PFOA, however, is quite challenging largely due to the ultra-high stability of C-F bonds. Compared with other techniques, photocatalytic degradation offers the potential advantages of simple operation under mild conditions as well as exceptional decomposition and defluorination efficiency. Titanium dioxide (TiO2) is one of the most frequently used photocatalysts, but so far, the pristine nanosized TiO2 (e.g., the commercial P25) has been considered inefficient for PFOA degradation, since the photo-generated hydroxyl radicals from TiO2 are not able to directly attack C-F bonds. Mesoporous Sb2O3/TiO2 heterojunctions were therefore rationally designed in this work, of which the confined Sb2O3 nanoparticles in mesoporous TiO2 framework could not only tune the band structure and also increase the number of active sites for PFOA degradation. It was found that, after loading Sb2O3, the absorption of UV light was enhanced, indicating a higher efficiency of light utilization; while the band gap was reduced, which accelerated the separation of photo-generated charge carriers; and most importantly, the valence band edge of the Sb2O3/TiO2 heterojunction was significantly lifted so as to prevent the occurrence of hydroxyl radical pathway. Under the optimal ratio of Sb2O3–TiO2, the resulting catalysts managed to remove 81.7% PFOA in 2 h, with a degradation kinetics 4.2 times faster than the commercial P25. Scavenger tests and electron spin resonance spectra further revealed that such improvement was mainly attributed to the formation of superoxide radicals and photo-generated holes, in which the former drove the decarboxylation from C7F15COOH–C7F15•, and the latter promoted the direct electron transfer for the conversion of C7F15COO−–C7F15COO•. The Sb2O3/TiO2 photocatalysts were highly recyclable, with nearly 90% of the initial activity being retained after five consecutive cycles, guaranteeing the feasibility of long-term operation.

Seasonal variation of water-column light utilization efficiency for primary production in Saroma-ko Lagoon

In Saroma-ko Lagoon, where scallop aquaculture is a thriving commercial activity, monitoring primary production is essential for determining the amount of scallops that can be farmed. Using the primary production data obtained so far, we calculated Ψ, an index of water-column light utilization efficiency, and clarified its seasonal variation. Ψ tended to be lower in the spring bloom season (February–April), and higher in the late autumn to winter (October–December). Low chlorophyll-normalized production, an index of growth rate, resulted in lower values, while low daily irradiance resulted in higher values. The values of Ψ from our study had a range of 0.05–1.42 gC gChl-a−1 mol photons−1 m2 (N = 56). These values were within the previously reported range of 0.07–1.92 (gC gChl-a−1 mol photons−1 m2) for seawater and fresh water worldwide. Therefore, it is likely that Ψ varies from 0.05–2 gC gChl-a−1 mol photons−1 m2, being affected by conditions of phytoplankton growth and sunlight intensity, regardless of whether samples are collected from seawater or fresh water. Using the median Ψ value of 0.45 gC gChl-a−1 mol photons−1 m2 obtained in this study, primary production was 0.3–3.5 times the actual production at Saroma-ko Lagoon. Using this method, primary production can be easily and constantly monitored, facilitating the sustainable development of scallop aquaculture.