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Calculating annual deposition

Sr calculated by dividing the annual deposit gauge collection by the average air concentration. The contribution of dry deposition to the deposit gauge is in fact usually ignored in calculating the washout ratio. Hence the velocity of deposition by washout is... [Pg.93]

The average concentration of phosphorus was found to be 3000 ppm. Given the calculated yearly material deposition rate, approximately 11 kg phosphorus would have been contributed each year. Cook and Heizer arrived at an annual deposition rate of 124 kg phosphorus to a site area by a standard population of 100 individuals (28). By utilizing this rate, a population of only nine individuals would have been required to account for the amounts of phosphorus found to be present. Because phosphorus as phosphate is the least mobile of the elements tested, this figure can be considered to represent an absolute minimum permanent population estimate for the site during the period of occupation under consideration. It should be remembered, however, that soil phosphate is also found in occluded forms and in organic combination and that these fractions were not totally measured by the procedure utilized (29). Consequently, the minimum population estimate should be increased, perhaps by as much as 50-60%, to about 15 individuals. [Pg.74]

Now that we have all the necessary tools, we turn our attention to the question we asked earlier about how much mon you need to put aside every year for the next five years to have 2000 fi)r the down payment of your car when you graduate. Recall that the interest rate is 6.5% compounding annually. The annual deposits are calculated from Equation (20.13), which leads to the following amount ... [Pg.607]

To directly compare the two sites, annual deposition fluxes were calculated. For each 9-day collection, the flux was calculated from the measured concentration and the amount of rain i.e. ... [Pg.217]

Atmospheric emissions of sulphur dioxide are either measured or estimated at their source and are thus calculated on a provincial or state basis for both Canada and the United States (Figure 2). While much research and debate continues, computer-based simulation models can use this emission information to provide reasonable estimates of how sulphur dioxide and sulphate (the final oxidized form of sulphur dioxide) are transported, transformed, and deposited via atmospheric air masses to selected regions. Such "source-receptor" models are of varying complexity but all are evaluated on their ability to reproduce the measured pattern of sulphate deposition over a network of acid rain monitoring stations across United States and Canada. In a joint effort of the U.S. Environmental Protection Agency and the Canadian Atmospheric Environment Service, eleven linear-chemistry atmospheric models of sulphur deposition were evaluated using data from 1980. It was found that on an annual basis, all but three models were able to simulate the observed deposition patterns within the uncertainty limits of the observations (22). [Pg.45]

Fig. 4-13 Calculated and observed annual wet deposition of sulfur in mgS/m per year. (Reprinted from "Atmospheric Environment," Volume 30, Feichter, J., Kjellstrom, E., Rodhe, H., Dentener, F., Lelieveld, and Roelofs, G.-J., Simulation of the tropospheric sulfur cycle in a global climate model, pp. 1693-1707, Copyright 1996, with permission from Elsevier Science.)... Fig. 4-13 Calculated and observed annual wet deposition of sulfur in mgS/m per year. (Reprinted from "Atmospheric Environment," Volume 30, Feichter, J., Kjellstrom, E., Rodhe, H., Dentener, F., Lelieveld, and Roelofs, G.-J., Simulation of the tropospheric sulfur cycle in a global climate model, pp. 1693-1707, Copyright 1996, with permission from Elsevier Science.)...
James AC. 1878. Lung deposition of sub-micron aerosols calculated as a function of age and breathing rate. In National Radiological Protection Board annual Research and Development Report. National Radiological Protection Board. Harwell, United Kingdom,71-75. [Pg.243]

The calculated maps of the annual mercury deposition in the Northern Hemisphere and over the considered countries are shown in Figure 13. A high transport ability of mercury enables it to be transported in the atmosphere over long distances. A significant part of mercury emitted in the polluted regions is deposited far from major... [Pg.372]

The distribution of the annual emissions of PCDD/F in the atmosphere of the F.MFP region in 2001 as compared with their distribution between different environmental compartments by the end of the calculated period is presented in Figure 7. Only 1 % of the annual PCDD/F emissions remains in the atmosphere about 56% are deposited to other media. However, the distribution between media after a long time period is not directly determined by PCDD/Fs depositions in 2001. To a great extent it results from their long-term accumulation in the environment (1970-2001). For example, the annual contribution of PCDD/Fs total emissions to soil is about 47%. However, after a long time period the most part of the total PCDD/Fs content in the environment (about 95%) accumulated in soil due to relatively low degradation rates for this medium. Thus, soil is the main medium-accumulator of PCDD/Fs. [Pg.389]

Nonetheless, methylmercury production can be proportional to Hg concentration (83, 89) and may be limited in lakes by the flux of reactive Hg(II) species across the sediment-water interface (52). Thus an increase in total Hg deposition could produce an equivalent response in Hg bioaccumulation, all other factors being equal. It may be significant in this regard that the average rate of increase in Hg residues in fish in Minnesota is of the same magnitude as that calculated here for atmospheric loading, roughly 3% annually since 1930 (19). [Pg.64]

Transport by Calcite. The annual flux of calcite into the uppermost trap (29 m below the lake surface) was estimated to be 35 g/m2, and the mean measured P content of this phase was estimated at 1.05 mg/g. A comparison of the calculated 29-m P flux, 37 mg/m2, with estimates of deposition to bottom sediment, indicated that 5-16 mg/m2 (13-43% of upper-water-column flux) was returned to the water column. This relatively small regeneration flux was not detected in profiles of meta- and hypolimnetic... [Pg.310]

Net sedimentation is defined as the flux of material incorporated into the permanent sediment record. 210Pb and 137Cs geochronologies indicate a mass sedimentation rate of 103 g/m2 per year for profundal sediments in Little Rock Lake. By using the mean Hg concentration (118 ng/g) in the top 1-cm slice of our bulk sediment profile, we estimated an annual net sedimentation of 12 xg of HgT/m2 per year. This net accumulation rate is similar to the calculated atmospheric input rate of about 10 xg/m2 per year (18, 19). Additionally, gross deposition rates (from sediment traps) exceeded these estimates by about a factor of 3 this rate suggests substantial internal recycling of material deposited at the sediment-water interface in this lake. [Pg.441]

Because of the unusual amount of dust deposited and because the dust came from an area that has received heavy annual treatment with pesticides for many years, a large sample was collected for analysis at an installation that had previously been used to collect rainfall. Essentially, the collection surface is one fourth of a galvanized iron roof with the gutter arranged to discharge roof runoff into a collection tank. The collection area is 1090 square feet calculated from a horizontal projection. The day after the storm, the roof surface was flushed with 110 liters of Cincinnati tap water, and the dust slurry was collected in a stainless steel tank. The roof surface had been cleansed before the dust was de-... [Pg.176]

Simple Interest interest is calculated with the formula I = PRT. The amount of money deposited is called the principal, P. The annual interest rate is represented by R, and T represents the time in years. [Pg.233]

In freshwater ecosystems, the amounts of phosphorus introduced to sediments are estimated to be of the order of 1 Tg P y while the amounts released from sediments annually are estimated to be less than 1 Tg P (Pierrou, 1976). Emery et al. (1955) calculated that the amount of phosphorus deposited in ocean sediments is 13 Tg P y. The amount of phosphorus released from ocean sediments is unknown but is probably relatively small, as the reducing conditions (lack of oxygen) required occur relatively rarely in the ocean. The uptake of phosphorus by phytoplankton in the ocean has been variously calculated as 1300 Tg P y (Emery et al., 1955) and 990 Tg P y (Stumm, 1973). A similar estimate, about 1000 Tg P y, can be made for the amount of phosphorus deposited in oceanic detritus (Pierrou, 1976). [Pg.208]

The metal soil concentrations provided in the problem statement correspond to those calculated in part 6. (The probability of contamination would otherwise be obtained by linear interpolation.) The annual probability of an individual dying a carcinogenic death from metal deposition over a 30-year period is therefore given by the product of the probabilites provided in (a), (b), and (c), in part 7 of the problem statement. [Pg.857]

To support the positive trend between 1993 and 1999, a simple scenario with Cd input and flux data for the whole Baltic Sea was estimated (Pohl and Hennings, 2005), leading to a Cddiss increase of 0.0105 nmol/(kg year) in Baltic Sea surface waters. Compared to the annual Cdjiss increase of0.0074 nmol/(kg year) between 1993 and 1999 as calculated above, this is a realistic value considering that data for atmospheric deposition, river input, and particulate export are still tenuous. [Pg.378]

Water soluble inorganic zinc species are predominant in the global ocean waters. It has been calculated that 90% of suspended and 35% of solnble riverine zinc are deposited at the ocean-land interface (Lisitsin et al, 1983). It leads to the annual accumulation of 0.6 X 10 tons ofZn in suspension and abontO.5 x 10 tons in soluble form in the pelagic part of the ocean. The average concentration of solnble Zn in the global marine waters is abont 5 /xg/L, with relevant amonnt in ocean water of 6, 800 x 10 tons. The suspended Zn amonnt is not estimated qnantitatively yet. [Pg.173]


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See also in sourсe #XX -- [ Pg.217 , Pg.219 ]




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