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  • 1
    Publication Date: 2024-02-07
    Description: Nitric oxide (NO) is an atmospheric pollutant and climate forcer as well as a key intermediary in the marine nitrogen cycle, but the ocean’s NO contribution and production mechanisms remain unclear. Here, high-resolution NO observations were conducted simultaneously in the surface ocean and the lower atmosphere of the Yellow Sea and the East China Sea; moreover, NO production from photolysis and microbial processes was analyzed. The NO sea–air exchange showed uneven distributions (RSD = 349.1%) with an average flux of 5.3 ± 18.5 × 10–17 mol cm–2 s–1. In coastal waters where nitrite photolysis was the predominant source (89.0%), NO concentrations were remarkably higher (84.7%) than the overall average of the study area. The NO from archaeal nitrification accounted for 52.8% of all microbial production (11.0%). We also examined the relationship between gaseous NO and ozone which helped identify sources of atmospheric NO. The sea-to-air flux of NO in coastal waters was narrowed by contaminated air with elevated NO concentrations. These findings indicate that the emissions of NO from coastal waters, mainly controlled by reactive nitrogen inputs, will increase with the reduced terrestrial NO discharge.
    Type: Article , PeerReviewed
    Format: text
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  • 2
    Publication Date: 2024-02-07
    Description: Nitric oxide (NO) is a short-lived intermediate of the oceanic nitrogen cycle, and it is produced by biological and photochemical processes in the ocean. Nitrogen dioxide (NO2) is a reactive atmospheric compound which has not been determined in the ocean so far. Here, we present the setup and validation of a novel continuous underway measurement system to measure dissolved NO and NO2 in the surface ocean. The system consists of a seawater/gas equilibration component coupled to a chemiluminescence detector. It was successfully deployed during a 12 day cruise to the East China Sea in May 2018. Dissolved NO and NO2 surface concentrations ranged from 〈limit of detection (LOD) to 98 × 10-12 mol L-1 and 〈LOD to 83 × 10-12 mol L-1, respectively. The ECS was supersaturated with NO but significantly undersaturated with NO2, indicating that the surface waters were a source for atmospheric NO but a sink for atmospheric NO2 at the time of our measurements.
    Type: Article , PeerReviewed
    Format: text
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