In many oceanic regions, anthropogenic warming will coincide with iron (Fe) limitation. Interactive effects between warming and Fe limitation on phytoplankton physiology and biochemical function are likely, as temperature and Fe availability affect many of the same essential cellular pathways. However, we lack a clear understanding of how globally significant phytoplankton such as the picocyanobacteria
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Synechococcus will respond to these co-occurring stressors, and what underlying molecular mechanisms will drive this response. Moreover, ecotype-specific adaptations can lead to nuanced differences in responses between strains. In this study,Synechococcus isolates YX04-1 (oceanic) and XM-24 (coastal) from the South China Sea were acclimated to Fe limitation at two temperatures, and their physiological and proteomic responses were compared. Both strains exhibited reduced growth due to warming and Fe limitation. However, coastal XM-24 maintained relatively higher growth rates in response to warming under replete Fe, while its growth was notably more compromised under Fe limitation at both temperatures compared with YX04-1. In response to concurrent heat and Fe stress, oceanic YX04-1 was better able to adjust its photosynthetic proteins and minimize the generation of reactive oxygen species while reducing proteome Fe demand. Its intricate proteomic response likely enabled oceanic YX04-1 to mitigate some of the negative impact of warming on its growth during Fe limitation. Our study highlights how ecologically-shaped adaptations inSynechococcus strains even from proximate oceanic regions can lead to differing physiological and proteomic responses to these climate stressors.Free, publicly-accessible full text available February 20, 2025 -
Abstract In this paper, Salen‐Ni basis polyphosphazene microsphere (Salen‐PZN‐Ni), boric acid (BA), and 3‐aminopropyltriethoxysilane (KH‐550) were used as raw materials to prepare a new flame retardant Salen‐PZN‐Ni@BA@KH‐550 by surface modification. The thermal and flame retardant properties of epoxy resin (EP) composites were studied. The introduction of Salen‐PZN‐Ni@BA@KH‐550 refined the thermal stability of EP composites, as well as the amount of carbon residue at 800°C. At 5 wt% of Salen‐PZN‐Ni@BA@KH‐550, the limiting oxygen index (LOI) of EP composites is increased from 25.4% to 30.5% and UL‐94 has been achieved with a V‐1 rating. Meanwhile, the mechanical properties of Salen‐PZN‐Ni@BA@KH‐550/EP composites were also improved. In addition, the good char formation ability of Salen‐PZN‐Ni@BA@KH‐550 caused the reduction of peak heat release rate, total heat release rate, maximum average heat release rate and total smoke generation of the EP composites. All these results indicate that Salen‐PZN‐Ni@BA@KH‐550/EP composites have a wider range of applications.
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NA (Ed.)
Abstract. Measurements of dissolved organic carbon (DOC), nitrogen (DON), and phosphorus (DOP) concentrations are used to characterize the dissolved organic matter (DOM) pool and are important components of biogeochemical cycling in the coastal ocean. Here, we present the first edition of a global database (CoastDOM v1; available at https://doi.org/10.1594/PANGAEA.964012, Lønborg et al., 2023) compiling previously published and unpublished measurements of DOC, DON, and DOP in coastal waters. These data are complemented by hydrographic data such as temperature and salinity and, to the extent possible, other biogeochemical variables (e.g. chlorophyll a, inorganic nutrients) and the inorganic carbon system (e.g. dissolved inorganic carbon and total alkalinity). Overall, CoastDOM v1 includes observations of concentrations from all continents. However, most data were collected in the Northern Hemisphere, with a clear gap in DOM measurements from the Southern Hemisphere. The data included were collected from 1978 to 2022 and consist of 62 338 data points for DOC, 20 356 for DON, and 13 533 for DOP. The number of measurements decreases progressively in the sequence DOC > DON > DOP, reflecting both differences in the maturity of the analytical methods and the greater focus on carbon cycling by the aquatic science community. The global database shows that the average DOC concentration in coastal waters (average ± standard deviation (SD): 182±314 µmol C L−1; median: 103 µmol C L−1) is 13-fold higher than the average coastal DON concentration (13.6±30.4 µmol N L−1; median: 8.0 µmol N L−1), which is itself 39-fold higher than the average coastal DOP concentration (0.34±1.11 µmol P L−1; median: 0.18 µmol P L−1). This dataset will be useful for identifying global spatial and temporal patterns in DOM and will help facilitate the reuse of DOC, DON, and DOP data in studies aimed at better characterizing local biogeochemical processes; closing nutrient budgets; estimating carbon, nitrogen, and phosphorous pools; and establishing a baseline for modelling future changes in coastal waters.
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Abstract Recent years have witnessed the rapid development of sustainable materials. Along this line, developing biodegradable or recyclable soft electronics is challenging yet important due to their versatile applications in biomedical devices, soft robots, and wearables. Although some degradable bulk hydrogels are directly used as the soft electronics, the sensing performances are usually limited due to the absence of distributed conducting circuits. Here, sustainable hydrogel‐based soft electronics (HSE) are reported that integrate sensing elements and patterned liquid metal (LM) in the gelatin–alginate hybrid hydrogel. The biopolymer hydrogel is transparent, robust, resilient, and recyclable. The HSE is multifunctional; it can sense strain, temperature, heart rate (electrocardiogram), and pH. The strain sensing is sufficiently sensitive to detect a human pulse. In addition, the device serves as a model system for iontophoretic drug delivery by using patterned LM as the soft conductor and electrode. Noncontact detection of nearby objects is also achieved based on electrostatic‐field‐induced voltage. The LM and biopolymer hydrogel are healable, recyclable, and degradable, favoring sustainable applications and reconstruction of the device with new functions. Such HSE with multiple functions and favorable attributes should open opportunities in next‐generation electronic skins and hydrogel machines.
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Abstract Sn‐based materials are identified as promising catalysts for the CO2electroreduction (CO2RR) to formate (HCOO−). However, their insufficient selectivity and activity remain grand challenges. A new type of SnO2nanosheet with simultaneous N dopants and oxygen vacancies (
V O‐rich N‐SnO2NS) for promoting CO2conversion to HCOO−is reported. Due to the likely synergistic effect of N dopant andV O, theV O‐rich N‐SnO2NS exhibits high catalytic selectivity featured by an HCOO−Faradaic efficiency (FE) of 83% at− 0.9 V and an FE of> 90% for all C1 products (HCOO−and CO) at a wide potential range from −0.9 to− 1.2 V. Low coordination Sn–N moieties are the active sites with optimal electronic and geometric structures regulated byV Oand N dopants. Theoretical calculations elucidate that the reaction free energy of HCOO* protonation is decreased on theV O‐rich N‐SnO2NS, thus enhancing HCOO−selectivity. The weakened H* adsorption energy also inhibits the hydrogen evolution reaction, a dominant side reaction during the CO2RR. Furthermore, using the catalyst as the cathode, a spontaneous Galvanic Zn‐CO2cell and a solar‐powered electrolysis process successfully demonstrated the efficient HCOO−generation through CO2conversion and storage.