Little is known about the combined impacts of future CO 2 and temperature increases on the growth and physiology of marine picocyanobacteria. We incubated Synechococcus and Prochlorococcus under present-day (380 ppm) or predicted year-2100 CO 2 levels (750 ppm), and under normal versus elevated temperatures (+4°C) in semicontinuous cultures. Increased temperature stimulated the cell division rates of Synechococcus but not Prochlorococcus. Doubled CO 2 combined with elevated temperature increased maximum chl a-normalized photosynthetic rates of Synechococcus four times relative to controls. Temperature also altered other photosynthetic parameters (a, F max , E k , and DF =F 0 m ) in Synechococcus, but these changes were not observed for Prochlorococcus. Both increased CO 2 and temperature raised the phycobilin and chl a content of Synechococcus, while only elevated temperature increased divinyl chl a in Prochlorococcus. Cellular carbon (C) and nitrogen (N) quotas, but not phosphorus (P) quotas, increased with elevated CO 2 in Synechococcus, leading to 20% higher C:P and N:P ratios. In contrast, Prochlorococcus elemental composition remained unaffected by CO 2 , but cell volume and elemental quotas doubled with increasing temperature while maintaining constant stoichiometry. Synechococcus showed a much greater response to CO 2 and temperature increases for most parameters measured, compared with Prochlorococcus. Our results suggest that global change could influence the dominance of Synechococcus and Prochlorococcus ecotypes, with likely effects on oligotrophic food-web structure. However, individual picocyanobacteria strains may respond quite differently to future CO 2 and temperature increases, and caution is needed when generalizing their responses to global change in the ocean.

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Organic–inorganic lead halide perovskite solar cells have realized a rapid increase of power conversion efficiency (PCE) in the past few years. However, their performance still suffers trap‐assisted decline due to defects at the surface and grain boundaries of the perovskite film. Herein, a phenethylammonium iodide‐lead iodide (PEAI‐PbI2) passivation layer is formed on the CH3NH3PbI3 perovskite film. The characterization results indicate that the PEAI covering layer leads to the reduction of surface defects and suppression of nonradiative recombination. By manipulating this surface passivation method, a remarkably improved VOC of 1.16 V and an enhanced PCE of 20.8% are achieved.

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