Joseph M. Prospero

The atmospheric input of trace species to the world ocean

Over the past decade it has become apparent that the atmosphere is a significant pathway for the transport of many natural and pollutant materials from the continents to the ocean. The atmospheric input of many of these species can have an impact (either positive or negative) on biological processes in the sea and on marine chemical cycling. For example, there is now evidence that the atmosphere may be an important transport path for such essential nutrients as iron and nitrogen in some regions. In this report we assess current data in this area, develop global scale estimates of the atmospheric fluxes of trace elements, mineral aerosol, nitrogen species, and synthetic organic compounds to the ocean; and compare the atmospheric input rates of these substances to their input via rivers. Trace elements considered were Pb, Cd, Zn, Cu, Ni, As, Hg, Sn, Al, Fe, Si, and P. Oxidized and reduced forms of nitrogen were considered, including nitrate and ammonium ions and the gaseous species NO, NO2, HNO3, and NH3. Synthetic organic compounds considered included polychlorinated biphenyls (PCBs), hexachlorocyclohexanes (HCHs), DDTs, chlordane, dieldrin, and hexachlorobenzenes (HCBs). Making this assessment was difficult because there are very few actual measurements of deposition rates of these substances to the ocean. However, there are considerably more data on the atmospheric concentrations of these species in aerosol and gaseous form. Mean concentration data for 10° × 10° ocean areas were determined from the available concentration data or from extrapolation of these data into other regions. These concentration distributions were then combined with appropriate exchange coefficients and precipitation fields to obtain the global wet and dry deposition fluxes. Careful consideration was given to atmospheric transport processes as well as to removal mechanisms and the physical and physicochemical properties of aerosols and gases. Only annual values were calculated. On a global scale atmospheric inputs are generally equal to or greater than riverine inputs, and for most species atmospheric input to the ocean is significantly greater in the northern hemisphere than in the southern hemisphere. For dissolved trace metals in seawater, global atmospheric input dominates riverine input for Pb, Cd, and Zn, and the two transport paths are roughly equal for Cu, Ni, As, and Fe. Fluxes and basin-wide deposition of trace metals are generally a factor of 5-10 higher in the North Atlantic and North Pacific regions than in the South Atlantic and South Pacific. Global input of oxidized and reduced nitrogen species are roughly equal to each other, although the major fraction of oxidized nitrogen enters the ocean in the northern hemisphere, primarily as a result of pollution sources. Reduced nitrogen species are much more uniformly distributed, suggesting that the ocean itself may be a significant source. The global atmospheric input of such synthetic organic species as HCH,PCBs, DDT, and HCB completely dominates their input via rivers.

Sources and distributions of dust aerosols simulated with the GOCART model

The global distribution of dust aerosol is simulated with the Georgia Tech/Goddard Global Ozone Chemistry Aerosol Radiation and Transport (GOCART) model. In this model all topographic lows with bare ground surface are assumed to have accumulated sediments which are potential dust sources. The uplifting of dust particles is expressed as a function of surface wind speed and wetness. The GOCART model is driven by the assimilated meteorological fields from the Goddard Earth Observing System Data Assimilation System (GEOS DAS) which facilitates direct comparison with observations. The model includes seven size classes of mineral dust ranging from 0.1–6 μm radius. The total annual emission is estimated to be between 1604 and 1960 Tg yr−1 in a 5-year simulation. The model has been evaluated by comparing simulation results with ground-based measurements and satellite data. The evaluation has been performed by comparing surface concentrations, vertical distributions, deposition rates, optical thickness, and size distributions. The comparisons show that the model results generally agree with the observations without the necessity of invoking any contribution from anthropogenic disturbances to soils. However, the model overpredicts the transport of dust from the Asian sources to the North Pacific. This discrepancy is attributed to an overestimate of small particle emission from the Asian sources.

Indian Ocean Experiment: An integrated analysis of the climate forcing and effects of the great Indo-Asian haze

Every year, from December to April, anthropogenic haze spreads over most of the North Indian Ocean, and South and Southeast Asia. The Indian Ocean Experiment (INDOEX) documented this Indo-Asian haze at scales ranging from individual particles to its contribution to the regional climate forcing. This study integrates the multiplatform observations (satellites, aircraft, ships, surface stations, and balloons) with one- and four-dimensional models to derive the regional aerosol forcing resulting from the direct, the semidirect and the two indirect effects. The haze particles consisted of several inorganic and carbonaceous species, including absorbing black carbon clusters, fly ash, and mineral dust. The most striking result was the large loading of aerosols over most of the South Asian region and the North Indian Ocean. The January to March 1999 visible optical depths were about 0.5 over most of the continent and reached values as large as 0.2 over the equatorial Indian ocean due to long-range transport. The aerosol layer extended as high as 3 km. Black carbon contributed about 14% to the fine particle mass and 11% to the visible optical depth. The single-scattering albedo estimated by several independent methods was consistently around 0.9 both inland and over the open ocean. Anthropogenic sources contributed as much as 80% (±10%) to the aerosol loading and the optical depth. The in situ data, which clearly support the existence of the first indirect effect (increased aerosol concentration producing more cloud drops with smaller effective radii), are used to develop a composite indirect effect scheme. The Indo-Asian aerosols impact the radiative forcing through a complex set of heating (positive forcing) and cooling (negative forcing) processes. Clouds and black carbon emerge as the major players. The dominant factor, however, is the large negative forcing (-20±4 W m^(−2)) at the surface and the comparably large atmospheric heating. Regionally, the absorbing haze decreased the surface solar radiation by an amount comparable to 50% of the total ocean heat flux and nearly doubled the lower tropospheric solar heating. We demonstrate with a general circulation model how this additional heating significantly perturbs the tropical rainfall patterns and the hydrological cycle with implications to global climate.

Long-Range Atmospheric Transport of Soil Dust from Asia to the Tropical North Pacific: Temporal Variability

The concentration of airborne soil dust at Enewetak Atoll(11�N, 162�E) in April 1979 was 2.3 micrograms per cubic meter but decreased steadily to 0.02 microgram per cubic meter over the next 5 months. The spring dust is probably derived from China; its deposition rate (∼0.3 millimeter per 1000 years) suggests that it may be a significant contributor to the deep-sea sediments of the North Pacific.

Characterization of tropospheric aerosols over the oceans with the NOAA advanced very high resolution radiometer optical thickness operational product

The National Oceanic and Atmospheric Administration (NOAA) advanced very high resolution radiometer (AVHRR) is an instrument on a polar orbiting satellite that provides information on global aerosol distributions. The remote sensing algorithm is based on measurements of backscattered solar radiation which yield a measure of the radiatively equivalent aerosol optical thickness τ A sat (EAOT) over the oceans. Seasonally composited EAOT data for the period July 1989 to June 1991 reveal many spatially coherent plume-like patterns that can usually be interpreted in terms of known (or reasonably hypothesized) sources in association with climatological wind fields. The largest and most persistent areas of high EAOT values are associated with wind-blown dust and biomass burning sources; especially prominent are sources in Africa, the middle East, and the Asian subcontinent. Prominent plumes over the midlatitude North Atlantic are attributed to pollution emissions from North America and Europe. Large plumes attributed to pollution aerosols and dust from sources in Asia are clearly visible over the western and central North Pacific. On a global scale the annually averaged northern hemisphere EAOT values are about 1.7 times greater than those in the southern hemisphere. Considering each hemisphere separately, EAOT values in summer are about twice those in winter. Within the midlatitude band 30°-60° (i.e., where anthropogenic emissions are greatest) the summer/winter ratio is about 3. The temporal variability of monthly mean EAOT in specific ocean regions often shows characteristic seasonal patterns that are usually consistent with aerosol measurements made in the marine boundary layer. Nonetheless, there are features in the EAOT distributions that can not be readily interpreted at this time. The AVHRR EAOT distributions demonstrate that satellite products can serve as a useful tool for the planning and implementation of focused aerosol research programs and that they will be especially important in studies of climate-related processes.

Impacts of Atmospheric Anthropogenic Nitrogen on the Open Ocean

Increasing quantities of atmospheric anthropogenic fixed nitrogen entering the open ocean could account for up to about a third of the oceans external (nonrecycled) nitrogen supply and up to ∼3% of the annual new marine biological production, ∼0.3 petagram of carbon per year. This input could account for the production of up to ∼1.6 teragrams of nitrous oxide (N2O) per year. Although ∼10% of the oceans drawdown of atmospheric anthropogenic carbon dioxide may result from this atmospheric nitrogen fertilization, leading to a decrease in radiative forcing, up to about two-thirds of this amount may be offset by the increase in N2O emissions. The effects of increasing atmospheric nitrogen deposition are expected to continue to grow in the future.

The Large-Scale Movement of Saharan Air Outbreaks over the Northern Equatorial Atlantic

Abstract The intense and prolonged heating of air passing over the Sahara during the summer and early fall months forms a deep mixed layer which extends up to 15–20,000 ft during July, the warmest month. The dust-laden heated air emerges from West Africa as a series of large-scale anticyclonic eddies which move westward over the tropical Atlantic above the trade-wind moist layer, principally in the layer between 5000 and 15,000 ft (600–800 mb). Measurements made during BOMEX show that this Saharan air is characterized by high values of potential temperature, dust and radon-222 which confirm a desert origin. As the parcels of air within the layer proceed across the Atlantic the continuous fallout of particulate matter and the mixing at the base of the layer cause dust to be transferred to the lower levels where its concentration may become sufficiently great to produce dense haze at the surface over wide areas over the Atlantic and Caribbean in the latitude belt 10–25N. Nevertheless, measurements indicate ...

Long-term measurements of the transport of African mineral dust to the southeastern United States: Implications for regional air quality

Continuous daily aerosol sampling carried out at a coastal site in Miami, Florida, for the past 23 years shows that large quantities of African mineral dust are periodically carried into Florida every summer, yielding daily concentrations in the range of about 10 μg m−3 to 100 μg m−3. Dust events typically last several days or longer. The maximum dust concentration occurs in July (monthly mean, 16.3 μg m−3), but relatively high concentrations are also observed in June (8.4 μg m−3) and August (9.8 μg m−3). There is considerable year-to-year variability that is apparently linked to various meteorological factors including climate conditions in North Africa as manifested by drought. Satellite data show that African dust incursions are synoptic-scale events; consequently, they will impact a large region of the southern and eastern United States. The incursion of dust events over this large region, coupled with inputs from local emissions, could have important implications regarding regional air quality.

Relationships among aerosol constituents from Asia and the North Pacific during PEM‐West A

Aerosol particle samples collected from Asia and the North Pacific were analyzed to investigate the relationships among atmospheric sea salt, mineral aerosol, biogenic emissions (methanesulfonate (MSA)), and several anthropogenic substances (sulfate, nitrate, and various trace elements). These studies specifically focused on the sources for aerosol SO4= and on the long-range transport of continental materials to the North Pacific. Ground-based aerosol sampling was conducted at four coastal-continental sites: Hong Kong, Taiwan, Okinawa, and Cheju; and at three remote Pacific islands, Shemya, Midway, and Oahu. Non-sea-salt (nss) SO4= and MSA were uncorrelated at the East Asian sites presumably because pollution sources overwhelm the biogenic emissions of nss SO4=. At the coastal-continental sites, marine biogenic emissions accounted for only 10 to <5% of the total nss SO4=. In contrast, over the ocean the concentrations of nss SO4= and MSA were correlated (Midway r = 0.70; Oahu r = 0.59), and higher percentages of biogenic nss SO4= occurred, 55 and 70% at Oahu and Midway, respectively. The concentrations of nss SO4= and NO3− were correlated at Cheju, Hong Kong, Taiwan, Okinawa, Midway, and Oahu, indicating some similarities in their sources and the processes governing their transport; however, differences in the nss SO4=/NO3− ratios among sites suggest regional differences in the pollution component of the aerosol. At Shemya the concentrations of MSA during the summer (100 ng m−3 or more) are about 2 orders of magnitude higher than those in winter. The dimethylsulfide-derived fraction of the nss SO4= is highest in the summer when the monthly median nss SO4=/MSA ratios range from 2.7 to 4.5, i.e., comparable to the ratios observed over Antarctica and other high-latitude locations. However, the monthly median nss SO4=/MSA ratios increase, reaching 50 to 200 in the winter as productivity nearly ceases, and the biogenic fraction of nss SO4= at Shemya decreases dramatically; this suggests a strong seasonal pollution component to the sulfate aerosol. The meteorological conditions favoring the long-range transport of Asian dust to the North Pacific also lead to transport of anthropogenic materials. At Oahu the correlation between NO3− and Al (dust) was highly significant (r = 0.75; p < 0.001), while the correlations between nitrate and Al at the continental sites were low. These differences indicate that the composition of the air sampled at the coastal-continental stations may be quite different from the air transported to the remote ocean. This phenomenon also appeared to affect the relationship between nss SO4= and antimony. The correlations between nss SO4= and Sb were weak at the Asian sites but strong at the open ocean sites where the nss SO4=/Sb ratios were higher than those over the continent.

Long-term simulation of global dust distribution with the GOCART model: correlation with North Atlantic Oscillation

Global distribution of aeolian dust is simulated from 1981 to 1996 with the Global Ozone Chemistry Aerosol Radiation and Transport (GOCART) model. The results are compared with in situ measurements and satellite data. An index is calculated from the model results and the satellite viewing angles to allow quantitative comparison with the Total ozone mapping spectrometer (TOMS) absorbing aerosol index. The annual budget over the different continents and oceans are analyzed. The simulated annual emission varies from a minimum of 1950 Tg in 1996 to a maximum of 2400 Tg in 1988. Of these emissions, 65% is from North Africa and 25% from Asia. It is found that North America received twice as much dust from other continents than it emits per year. There is no significant trend over the 16-year simulation. The inter-annual variability of dust distribution is analyzed over the North Atlantic and Africa. It is found that in winter a large fraction of the North Atlantic and Africa dust loading is correlated with the North Atlantic Oscillation (NAO) index. It is shown that a controlling factor of such correlation can be attributed to dust emission from the Sahel. The Bodele depression is the major dust source in winter and its inter-annual variability is highly correlated with the NAO. However, the long record of dust concentration measured at Barbados indicates that there is no correlation with the NAO index and surface concentration in winter. Longer simulation should provide the information needed to understand if the effects of the NAO on dust distribution is rather limited or Barbados is at the edge of the affected region.  2003 Elsevier Ltd. All rights reserved.