Claire Hughes

Megacities and Large Urban Agglomerations in the Coastal Zone: Interactions Between Atmosphere, Land, and Marine Ecosystems

Megacities are not only important drivers for socio-economic development but also sources of environmental challenges. Many megacities and large urban agglomerations are located in the coastal zone where land, atmosphere, and ocean meet, posing multiple environmental challenges which we consider here. The atmospheric flow around megacities is complicated by urban heat island effects and topographic flows and sea breezes and influences air pollution and human health. The outflow of polluted air over the ocean perturbs biogeochemical processes. Contaminant inputs can damage downstream coastal zone ecosystem function and resources including fisheries, induce harmful algal blooms and feedback to the atmosphere via marine emissions. The scale of influence of megacities in the coastal zone is hundreds to thousands of kilometers in the atmosphere and tens to hundreds of kilometers in the ocean. We list research needs to further our understanding of coastal megacities with the ultimate aim to improve their environmental management.

Seasonal cycle of seawater bromoform and dibromomethane concentrations in a coastal bay on the western Antarctic Peninsula

Sea-to-air emissions of bromocarbon gases are known to play an important role in atmospheric ozone depletion. In this study, seawater concentrations of bromoform (CHBr3) and dibromomethane (CH2Br2) were measured regularly between February 2005 and March 2007 at the Rothera Oceanographic and Biological Time Series (RaTS) site located in Marguerite Bay on the Antarctic Peninsula. Strong seasonality in CHBr3 and CH2Br2 concentrations was observed. The highest bromocarbon concentrations (up to 276.4 +/- 13.0 pmol CHBr3 L-1 and 30.0 +/- 0.4 pmol CH2Br2 L-1) were found to coincide with the annual microalgal bloom during the austral summer, with lower concentrations (up to 39.5 pmol CHBr3 L-1 and 9.6 +/- 0.6 pmol CH2Br2 L-1) measured under the winter fast ice. The timing of the initial increase in bromocarbon concentrations was related to the sea-ice retreat and onset of the microalgal bloom. Observed seasonal variability in CH2Br2/CHBr3 suggests that this relationship may be of use in resolving bromocarbon source regions. Mainly positive saturation anomalies calculated for both the 2005/2006 and 2006/2007 summers suggest that the bay was a source of CHBr3 and CH2Br2 to the atmosphere. Estimates of bromocarbon sea-to-air flux rates from Marguerite Bay during ice-free periods are 84 (-13 to 275) CHBr3 nmol m(-2) d(-1) and 21 (2 to 70) nmol CH2Br2 m(-2) d(-1). If these flux rates are representative of the seasonal ice edge zone bloom which occurs each year over large areas of the Southern Ocean during the austral summer, sea-to-air bromocarbon emissions could have an important impact on the chemistry of the Antarctic atmosphere.

Volatile halocarbon emissions by three tropical brown seaweeds under different irradiances

The emission rates of eight volatile halogenated compounds by three tropical brown seaweed species collected from Cape Rachado, west coast Peninsular Malaysia, under different irradiances have been determined. A purge-and-trap sample preparation system with a gas chromatograph and mass-selective detector was used to measure a suite of halocarbons released by Sargassum binderi Sonder ex J. Agardh, Padina australis Hauck, and Turbinaria conoides (J. Agardh) Kützing. All species are widely distributed in Peninsular Malaysia, with S. binderi a dominant seaweed species at our survey site. Release of few halocarbons was found to be influenced by irradiance. Correlations were also observed between emission of certain halocarbons with photosynthetic activity, especially bromo-and iodinated compounds (0.6 < r <0.9; p < 0.01) suggesting that environmental factors such as light can affect the release of these volatile halogenated compounds by the seaweeds into the atmosphere. Compared with temperate and polar brown seaweeds, tropical species, such as T. conoides, may emit higher levels of bromoform, CHBr3, and other halocarbons. It is therefore important to investigate the contribution of tropical seaweeds towards the local atmospheric composition of halocarbons.

Short-Lived Trace Gases in the Surface Ocean and the Atmosphere

The two-way exchange of trace gases between the ocean and the atmosphere is important for both the chemistry and physics of the atmosphere and the biogeochemistry of the oceans, including the global cycling of elements. Here we review these exchanges and their importance for a range of gases whose lifetimes are generally short compared to the main greenhouse gases and which are, in most cases, more reactive than them. Gases considered include sulphur and related compounds, organohalogens, non-methane hydrocarbons, ozone, ammonia and related compounds, hydrogen and carbon monoxide. Finally, we stress the interactivity of the system, the importance of process understanding for modeling, the need for more extensive field measurements and their better seasonal coverage, the importance of inter-calibration exercises and finally the need to show the importance of air-sea exchanges for global cycling and how the field fits into the broader context of Earth System Science.

Methyl and ethyl nitrate saturation anomalies in the Southern Ocean (36–65°S, 30–70°W)

Environmental Context. The alkyl nitrates are a group of organic compounds that are known to be produced naturally in seawater. The sea-to-air flux of alkyl nitrates is believed to contribute significantly to the ‘odd nitrogen’ reservoir of the atmosphere and to play an important role in regulating tropospheric ozone levels in remote marine regions. Here we expand our knowledge of alkyl nitrate concentration distributions and saturation anomalies to Southern Ocean waters. Abstract. We report the first coupled atmosphere and seawater alkyl nitrate measurements for the Southern Ocean in the area bounded by 36–65°S, 30–70°W (November/December, 2004). Methyl and ethyl nitrate concentrations in seawater were 3.1–194.9 and 0.3–71.8 pmol L–1, respectively. Atmospheric mixing ratios ranged from 1.0 to 71.5 ppt for methyl nitrate and 0.6 to 16.6 ppt for ethyl nitrate. No correlations between alkyl nitrate distributions, and sea surface temperature, windspeed or chlorophyll a were observed. However, methyl and ethyl nitrate were well correlated in both the air and seawater, which suggests a common source. Calculations based on these observations estimate median saturation anomalies of –40% (–95 to 220%) for methyl nitrate and –11% (–98 to 174%) for ethyl nitrate. Positive saturation anomalies were spatially patchy, which suggests that some methyl and ethyl nitrate production was taking place in isolated areas of the study region. Overall our negative median saturation anomaly values suggest that during late austral spring (2004) the region of the Southern Ocean in which our measurements were made was not a net source of methyl or ethyl nitrate to the atmosphere. These results reinforce previous findings which suggest that whilst the equatorial ocean is a major source of methyl and ethyl nitrates to the atmosphere, higher latitude waters are generally at equilibrium or under-saturated. More measurements are required to assess how representative our results are of other areas of the Southern Ocean.