On biotic and abiotic drivers of the microphytobenthos seasonal cycle in a temperate intertidal mudflat: a modelling study

Microphytobenthos (MPB) from intertidal mudflats are key primary producers at the land–ocean interface. MPB can be more productive than phytoplankton and sustain both benthic and pelagic higher trophic levels. The objective of this study is to assess the contribution of light, mud temperature, and gastropod Peringia ulvae grazing pressure in shaping the seasonal MPB dynamics on the Brouage mudflat (NW France). We use a physical–biological coupled model applied to the sediment first centimetre for the year 2008. The simulated data compare to observations, including time-coincident remotely sensed and in situ data. The model suggests an MPB annual cycle characterised by a main spring bloom, a biomass depression in summer, and a moderate fall bloom. In early spring, simulated photosynthetic rates are high due to mud surface temperature (MST) values close to the MPB temperature optimum for photosynthesis and because increasing solar irradiance triggers the onset of the MPB spring bloom. Simulated peaks of high P. ulvae grazing (11 days during which ingestion rates exceed the primary production rate) mostly contribute to the decline of the MPB bloom along with the temperature limitation for MPB growth. In late spring–summer, the MPB biomass depression is due to the combined effect of thermo-inhibition and a moderate but sustained grazing pressure. The model ability to infer biotic and abiotic mechanisms driving the seasonal MPB dynamics could open the door to a new assessment of the export flux of biogenic matter from the coast to the open ocean and, more generally, of the contribution of productive intertidal biofilms to the coastal carbon cycle.

Seasonal observations of OH and HO₂ in the remote tropical marine boundary layer

Field measurements of the hydroxyl radical, OH, are crucial for our understanding of tropospheric chemistry. However, observations of this key atmospheric species in the tropical marine boundary layer, where the warm, humid conditions and high solar irradiance lend themselves favourably to production, are sparse. The Seasonal Oxidant Study at the Cape Verde Atmospheric Observatory in 2009 allowed, for the first time, seasonal measurements of both OH and HO2 in a clean (i.e. low NOx), tropical marine environment. It was found that concentrations of OH and HO2 were typically higher in the summer months (June, September), with maximum daytime concentrations of ~9 × 106 and 4 × 108 molecule cm−3, respectively – almost double the values in winter (late February, early March). HO2 was observed to persist at ~107 molecule cm−3 through the night, but there was no strong evidence of nighttime OH, consistent with previous measurements at the site in 2007. HO2 was shown to have excellent correlations (R2 ~ 0.90) with both the photolysis rate of ozone, J(O1D), and the primary production rate of OH, P(OH), from the reaction of O(1D) with water vapour. The analogous relations of OH were not so strong (R2 ~ 0.6), but the coefficients of the linear correlation with J(O1D) in this study were close to those yielded from previous works in this region, suggesting that the chemical regimes have similar impacts on the concentration of OH. Analysis of the variance of OH and HO2 across the Seasonal Oxidant Study suggested that ~70% of the total variance could be explained by diurnal behaviour, with ~30% of the total variance being due to changes in air mass.

Seasonal observations of OH and HO₂ in the remote tropical marine boundary layer

Field measurements of the hydroxyl radical, OH, are crucial for our understanding of tropospheric chemistry. However, observations of this key atmospheric species in the tropical marine boundary layer, where the warm, humid conditions and high solar irradiance lend themselves favourably to production, are sparse. The Seasonal Oxidant Study at the Cape Verde Atmospheric Observatory in 2009 allowed, for the first time, seasonal measurements of both OH and HO2 in a clean (i.e. low NOx), tropical marine environment. It was found that concentrations of OH and HO2 were typically higher in the summer months (June, September), with maximum daytime concentrations of ~9 × 106 and 4 × 108 molecule cm−3, respectively – almost double the values in winter (February, early March). HO2 was observed to persist at ~107 molecule cm−3 through the night, but there was no strong evidence of nighttime OH, consistent with previous measurements at the site in 2007. HO2 was shown to have excellent correlations (R2 ~ 0.90) with both the photolysis rate of ozone, J(O1D), and the primary production rate of OH, P(OH), from the reaction of O1D) with water vapour. The analogous relations of OH were not so strong (R2 ~ 0.6), but the coefficients of the linear correlation with J(O1D) in this study were close to those yielded from previous works in this region, suggesting that the chemical regimes have similar impacts on the concentration of OH. Analysis of the variance of OH and HO2 across the Seasonal Oxidant Study suggested that ~70 % of the total variance could be explained by diurnal behaviour, with ~30 % of the total variance being due to changes in air mass.