“Dynamics of chromophoric dissolved organic matter in the Atlantic Ocean: unravelling province-dependent relationships, optical complexity, and environmental influences”

Copyright \ua9 2024 Sabbaghzadeh, Uher and Upstill-Goddard.We report on the spatial distributions and optical characteristics of chromophoric dissolved organic matter (CDOM) in the sea surface microlayer (SML), subsurface seawater (SSW), and water column profiles down to 500 m across a range of Atlantic Ocean biogeochemical provinces during two cruises of the UK Atlantic Meridional Transect program (AMT24 and AMT25). We measured the CDOM absorption coefficient at 300 nm, aCDOM(300), and determined CDOM spectral slopes across two UV wavelength ranges: S1 (275-295 nm) and S2 (350-400 nm). We used spectral slope ratios (SR: S1/S2) to infer CDOM source characteristics and transformation history. During both cruises, SML aCDOM(300) was highest in the Northern Hemisphere, particularly in the North Atlantic Drift Region (NADR). CDOM was always enriched in the SML, with enrichment factors (SML aCDOM(300) / SSW aCDOM(300)) ranging from 1.03 to 2.00, reflecting preferential accumulation of CDOM in the SML. We also found a significant inverse correlation between aCDOM(300) and S1 in both the SML (Spearman’s rank correlation coefficient, r2 = -0.75, p < 0.001, n = 114) and water column profiles (r2 = -0.74, p < 0.001, n = 845). Biogeochemical province-dependent variations in the relationships between CDOM and chlorophyll a were also observed. In high-latitude regions, elevated aCDOM(300) and low SR values indicated a dominance of terrestrially-derived CDOM, whereas oligotrophic subtropical areas showed lower aCDOM(300) and higher SR values, suggestive of aged, refractory, and photodegraded biologically-derived CDOM. Taken together, these findings reveal a complexity of drivers affecting CDOM distributions and spectral properties, which may limit the use of CDOM in predictive relationships in the oceans. However, the potential use of chlorophyll a as a CDOM proxy may prove most successful in open ocean regions devoid of terrestrial inputs, where biological production predominates

Reduced air–sea CO2 exchange in the Atlantic Ocean due to biological surfactants

This is the author accepted manuscript. The final version is available from Springer Nature via the DOI in this recordOcean CO2 uptake accounts for 20–40% of the post-industrial sink for anthropogenic CO2. The uptake rate is the product of the CO2 interfacial concentration gradient and its transfer velocity, which is controlled by spatial and temporal variability in near-surface turbulence. This variability complicates CO2 flux estimates and in large part reflects variable sea surface microlayer enrichments in biologically derived surfactants that cause turbulence suppression. Here we present a direct estimate of this surfactant effect on CO2 exchange at the ocean basin scale, with derived relationships between its transfer velocity determined experimentally and total surfactant activity for Atlantic Ocean surface seawaters. We found up to 32% reduction in CO2 exchange relative to surfactant-free water. Applying a relationship between sea surface temperature and total surfactant activity to our results gives monthly estimates of spatially resolved ‘surfactant suppression’ of CO2 exchange. Large areas of reduced CO2 uptake resulted, notably around 20° N, and the magnitude of the Atlantic Ocean CO2 sink for 2014 was decreased by 9%. This direct quantification of the surfactant effect on CO2 uptake at the ocean basin scale offers a framework for further refining estimates of air–sea gas exchange up to the global scale.This work was supported by grants from the Leverhulme Trust to R.C.U.G. (RPG-303) and the UK Natural Environment Research Council (NERC) to R.C.U.G. (NE/K00252X/1) and J.D.S. (NE/K002511/1). Both NERC grants are components of RAGNARoCC (Radiatively Active Gases from the North Atlantic Region and Climate Change), which contributes to NERC's Greenhouse Gas Emissions and Feedbacks programme (www.nerc.ac.uk/research/funded/programmes/greenhouse). J.D.S. and I.A. acknowledge additional support from the European Space Agency (grant 4000112091/14/I-LG). R.P. acknowledges support from T. Wagner. This study is a contribution to the international IMBeR project and was supported by UK NERC National Capability funding to Plymouth Marine Laboratory and the National Oceanography Centre, Southampton. This is contribution no. 324 of the AMT programme

The Atlantic Ocean surface microlayer from 50°N to 50°S is ubiquitously enriched in surfactants at wind speeds up to 13 m s−1

We report the first measurements of surfactant activity (SA) in the sea surface microlayer (SML) and in subsurface waters (SSW) at the ocean basin scale, for two Atlantic Meridional Transect from cruises 50°N to 50°S during 2014 and 2015. Northern Hemisphere (NH) SA was significantly higher than Southern Hemisphere (SH) SA in the SML and in the SSW. SA enrichment factors (EF = SASML/SASSW) were also higher in the NH, for wind speeds up to ~13 m s−1, questioning a prior assertion that Atlantic Ocean wind speeds >12 m s−1 poleward of 30°N and 30°S would preclude high EFs and showing the SML to be self-sustaining with respect to SA. Our results imply that surfactants exert a control on air-sea CO2 exchange across the whole North Atlantic CO2 sink region and that the contribution made by high wind, high latitude oceans to air-sea gas exchange globally should be reexamined

EXTRACTION OF ASTAXANTHIN ESTERS FROM SHRIMP WASTE BY CHEMICAL AND MICROBIAL METHODS

The carotenoid pigments specifically astaxanthin has many significant applications in food, pharmaceutical and cosmetic industries. The goal of this research was the extraction of Astaxanthin from a certain Persian Gulf shrimp species waste (Penaeus semisulcatus), purification and identification of the pigment by chemical and microbial methods. Microbial fermentation was obtained by inoculation of two Lactobacillus species Lb. plantarum and Lb. acidophilus in the medium culture containing shrimp waste powder by the intervention of lactose sugar, yeast extract, the composition of Both and the coolage (-20°C). The carotenoids were extracted by an organic solvent system. After purification of astaxanthin with the thin layer chromatography method by spectrophotometer, NMR and IR analysis the presence of astaxanthin esters was recognized in this specific species of Persian Gulf shrimp. Results obtained from this study showed that the coolage at –20 °C not only does not have an amplifying effect on the production of astaxanthin but also slightly reduces this effect. Also the effect of intervention of lactose sugar showed more effectiveness in producing astaxanthin than yeast extract or more than with the presence of both. The results also indicated that there is not much difference in the ability of producing the pigment by comparing both Lb. plantarum and Lb. acidophillus. Also results showed the microbial method of extraction of astaxanthin is more effective than chemical method. The pigment extracted from certain amount of shrimp powder, 23.128 mg/g, was calculated

Meridional and Cross‐Shelf Variability of N2O and CH4 in the Eastern‐South Atlantic

Upward transport and/or mixing of trace gas-enriched subsurface waters fosters the exchange of nitrous oxide (N2O) and methane (CH4) with the atmosphere in the Eastern-South Atlantic (ESA). To date, it is, however, unclear whether this source is maintained by local production or advection of trace gas-enriched water masses. The meridional and zonal variability of N2O and CH4 in the ESA were investigated to identify the contributions of the major regional water masses to the overall budget of N2O and CH4. The maximal sea surface N2O and CH4 concentrations and the main ESA upwelling cells co-occurred with a strong negative correlation with the sea surface temperature (SST) (p < 0.05). The dominance of the central water masses in the winter and spring seasons and the interplay between shelf topography and wind regime are suggested to determine enhanced gas transfer toward the sea-air interface or “capping” at midwater depth. These parameters are supposed to be critical in the local budget of N2O and CH4 in the ESA. Our findings also show that the shape of N2O and CH4 gradients is very similar both meridionally and zonally; however, the extent of the differences between the high-end and low-end members of the concentrations/saturations range is different. This suggests a more pronounced effect of local sources on CH4 than N2O distribution, in particular in the Walvis Bay area. With respect to N2O, however, low-oxygen waters from the poleward undercurrent impinge in the shelf close to Cape Frio and often result in N2O concentrations significantly higher than off Lüderitz (p < 0.05