Aquatic chemistry is becoming both a rewarding and substantial area of inquiry and is drawing many prominent scientists to its fold. Its literature has changed from a compilation of compositional tables to studies of the chemical reactions occurring within the aquatic environments. But more than this is the recognition that human society in part is determining the nature of aquatic systems. Since rivers deliver to the world ocean most of its dissolved and particulate components, the interactions of these two sets of waters determine the vitality of our coastal waters. This significant vol ume provides not only an introduction to the dynamics of aquatic chem istries but also identifies those materials that jeopardize the resources of both the marine and fluvial domains. Its very title provides its emphasis but clearly not its breadth in considering natural processes. The book will be of great value to those environmental scientists who are dedicated to keeping the resources of the hydrosphere renewable. As the size of the world population becomes larger in the near future and as the uses of materials and energy show parallel increases, the rivers and oceans must be considered as a resource to accept some of the wastes of society. The ability of these waters and the sediments below them to accommodate wastes must be assessed continually. The key questions relate to the capacities of aqueous systems to carry one or more pollutants."

Metal pollution in the aquatic environment

The Environmental Protection Agency (EPA) provides access to information on a variety of topics related to the environment and strives to inform citizens of health risks. The EPA also has an extensive library network that consists of 26 libraries throughout the United States, which provide access to a plethora of information to EPA employees, scientists, and researchers. The EPA implemented a reorganization project to digitize their materials so they would be more accessible to a wider range of users, but this plan was drastically accelerated when the EPA was threatened with a budget cut. It chose to close and reduce the hours and services of some of their libraries. As a result, the agency was accused of denying users the “right to know” by making information unavailable, not providing an adequate strategic plan, and discarding vital materials. This case study explores the background of the digitization project, the practices implemented, and the critiques of the project.

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The Environmental Protection Agency

https://uhra.herts.ac.uk/bitstream/handle/2299/1986/901994.pdf?sequence=1

Atmospheric polycyclic aromatic hydrocarbons: Source attribution, emission factors and regulation

Fabry, V. J., Seibel, B. A., Feely, R. A., and Orr, J. C. 2008. Impacts of ocean acidification on marine fauna and ecosystem processes. - ICES Journal of Marine Science, 65: 414-432.Oceanic uptake of anthropogenic carbon dioxide (CO 2 ) is altering the seawater chemistry of the world’s oceans with consequences for marine biota. Elevated partial pressure of CO 2 (pCO 2 ) is causing the calcium carbonate saturation horizon to shoal in many regions, particularly in high latitudes and regions that intersect with pronounced hypoxic zones. The ability of marine animals, most importantly pteropod molluscs, foraminifera, and some benthic invertebrates, to produce calcareous skeletal structures is directly affected by seawater CO 2 chemistry. CO 2 influences the physiology of marine organisms as well through acid-base imbalance and reduced oxygen transport capacity. The few studies at relevant pCO 2 levels impede our ability to predict future impacts on foodweb dynamics and other ecosystem processes. Here we present new observations, review available data, and identify priorities for future research, based on regions, ecosystems, taxa, and physiological processes believed to be most vulnerable to ocean acidification. We conclude that ocean acidification and the synergistic impacts of other anthropogenic stressors provide great potential for widespread changes to marine ecosystems.

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Impacts of ocean acidification on marine fauna and ecosystem processes

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.

The atmospheric input of trace species to the world ocean

Determination of mercury in seawater at sub-nanogram per liter levels

Geochemistries of arsenic, antimony, mercury, and related elements in sediments of Puget Sound

The inhibition of marine nitrification by ocean disposal of carbon dioxide.

Polycyclic aromatic hydrocarbon (PAH) compositions were characterized monthly over a 1-year period in atmospheric particulate material (APM) collected from three locations in western Washington state and riverine suspended particulate material (SPM) collected near the mouth of the Columbia River. PAH mixtures of APM are dominated by compounds of combustion origin, with minor levels of the resin acid-derived PAH retene often present. SPM contained comparable levels of individual combustion PAH, retene, and perylene. Atmospheric and riverine contributions of individual combustion PAH to the Washington coastal environment were estimated from these data and other available information. Comparison of estimates with respective PAH accumulation rates measured in lead-210 dated coastal sediments shows that >30% of all combustion PAH, retene, and perylene in these sediments is supplied by SPM discharge from the Columbia River and direct atmospheric input accounts for at most 10% of the combustion PAH. Atmospherically transportable PAH are removed from the air over land to soils and freshwaters within the river drainage basin, eroded on particles, and discharged into the Washington coastal environment along with other nonatmospherically transportable PAH such as perylene as intrinsic constituents of the Columbia River's suspended sediment load.

Eric A. Crecelius

Papers

Determination of mercury in seawater at sub-nanogram per liter levels

Geochemistries of arsenic, antimony, mercury, and related elements in sediments of Puget Sound

The inhibition of marine nitrification by ocean disposal of carbon dioxide.

Polycyclic aromatic hydrocarbons in Washington coastal sediments: an evaluation of atmospheric and riverine routes of introduction

Distribution of silver, mercury, lead, copper and cadmium in central puget sound sediments