3.3.1. Mass Analysis
Inverted-disc sampling occurred during the sampling periods 21 April to 22 May 2014; and 11 June to 9 July 2014.
Table 1 shows the deposition fluxes (mass deposited per unit time and sampler surface area) for each disc sampler during both periods and the corresponding model predicted PM
27 deposition. It is important to point out that the model developed here predicts deposition of dust generated on the mine tailings and not total deposition, since the region has multiple potential dust sources. It is clear from the data in
Table 1 that the model under predicts total deposition, as expected.
Table 1.
Measured dust (PM27) mass deposition fluxes in inverted-disc samplers.
Table 1.
Measured dust (PM27) mass deposition fluxes in inverted-disc samplers.
Location | 4/21 to 5/22 Observed Deposition (mg/m2/day) | 4/21 to 5/22 Predicted Deposition (mg/m2/day) | 6/11 to 7/09 Observed Deposition (mg/m2/day) | 6/11 to 7/09 Predicted Deposition (mg/m2/day) |
---|
A | 15.6 | 7.69 | 17.0 | 4.48 |
B | 24.2 | 7.96 | 37.1 | 6.11 |
C | 6.9 | 6.04 | 26.1 | 4.66 |
D | 26.0 | 1.82 | 29.7 | 1.36 |
E | 9.4 | 4.48 | 12.1 | 0.53 |
F | 14.2 | 2.45 | 10.6 | 0.27 |
G | 12.3 | 8.11 | 8.5 | 8.21 |
H | 18.2 | 8.75 | 8.1 | 8.67 |
I | 10.1 | 7.39 | 12.6 | 7.02 |
J | 16.2 | 7.76 | 9.0 | 7.54 |
K | 30.0 | 5.47 | 17.3 | 5.16 |
L | 16.3 | 5.45 | 15.5 | 5.15 |
M | 16.0 | 1.06 | N/A | N/A |
N | 32.5 | 1.16 | 6.4 | 0.68 |
AA | N/A | N/A | 12.0 | 7.77 |
BB | N/A | N/A | 8.7 | 7.43 |
CC | N/A | N/A | 11.0 | 4.81 |
The highest deposition fluxes were measured at location N (
Figure 1) for the May sampling period and location B for the June sampling period. Sample N is located adjacent to the highway while sample B is located on the main tailings impoundment. Because roadways are well documented as production source of atmospheric aerosols, it follows that we would expect larger amounts of deposition to be captured with the N sampler.
The observed deposition flux for the two sampling periods is within an order of magnitude of the forecast deposition fluxes. The peak forecast deposition flux is approximately half of that measured using the samplers. However, the model forecast deposition fluxes drops dramatically for samplers located far from the tailings source (i.e., samplers F, M and N) while the total mass of dust measured by the samplers remains similar no matter their location. It is important to consider the fact that wind erosion occurs from a variety of sources within the region and each deposition sampler is collecting dust from all of them not just aerosols resulting from the tailings, although the exposed, elevated tailings are thought to be an important contributor.
As mentioned, the deposition forecasting model only simulates the transport of windblown particulate matter from the tailing impoundment and for particles with an aerodynamic diameter ≤27 μm. Comparing forecasts of PM
27 to bulk deposition samples has inherent errors caused by the potential of the samplers to collect larger particles and skewing the mass fluxes. In order to minimize these issues certain steps were taken to reduce the impact of large particles. The inverted-disc samplers were shown in wind tunnel tests to have the highest collection efficiency, up to 60%, for particles with diameter 10 to 31 μm. Their collection efficiency significantly drops for particles up to 89-μm [
21]. The samplers were placed at 1-m height to minimize the capture of large saltating particles. Additionally, mass fractions of dust measured by the MOUDI at 1-m height [
11] were 30.1%, 30.0%, and 39.9% for the >18-μm, 18 to 3.1-μm and <3.1-μm size fractions. The large percentage of mass observed in the smaller size fractions gives us confidence that the inverted-disc samplers are not significantly affected by larger particles and their results are reasonable approximations of PM
27 aerosol deposition.
Additional errors in the forecast depositions can arise from the DFM dependency on the WRF wind speed forecast. The WRF model provides us with the highest resolution weather forecasts of the region but it is still susceptible to errors including those experienced during short term high wind events. The compounding factors of multiple dust sources, DFM forecast of PM
27 and errors in the WRF forecast makes the under estimated DFM deposition fluxes measured by the inverted-disc samplers reasonable,
Table 1. Through the use of elemental analysis we can partition the captured dust and determine the relative influence the tailings have on each sampler and the relative spatial distributions.
3.3.2. Lead and Arsenic Analysis
The tailings and surrounding soil have significantly elevated arsenic and lead concentrations when compared to the natural surroundings [
14]. This is illustrated by the results in
Figure 7, where topsoil concentrations of lead and arsenic are shown as a function of distance from the tailings along a NE transect. Significant arsenic and lead contamination extend at least to 1 km from the tailings, while the 5 km site exhibits relatively low concentrations, which could correspond to background levels in the region (around 10 ppm for both arsenic and lead).
Figure 7.
Arsenic and lead concentrations in topsoil (0–3 mm depth) samples at different distances from the mine tailings following a NE transect. Error bars show standard deviation of triplicate samples at the same location.
Figure 7.
Arsenic and lead concentrations in topsoil (0–3 mm depth) samples at different distances from the mine tailings following a NE transect. Error bars show standard deviation of triplicate samples at the same location.
The arsenic and lead concentrations measured in inverted-disc samplers are presented in
Table 2.
Figure 8 and
Figure 9 show the DFM predictions of average deposition fluxes for the May and June sample periods. A way to assess the results is to compare transects of relative observed concentrations of As and Pb with forecast deposition of PM
27. Three transects are evaluated in the southwestward, eastward and northward directions. The relative Pb and As concentration transects are calculated by normalizing each sampler to the average concentration measured by inverted-disc samplers A and B located on the tailings pile. Equation (1) shows the normalization process for a sample concentration (C
sample) where C
A and C
B are the concentrations measured at samplers A and B, respectively. Transects of the DFM PM
27 are normalized by the forecast deposition at the location of sampler B (34.50087° latitude and −112.25305° longitude). All distances of the sample locations are calculated from sample point B.
The southward transect is generated using the normalized samples A and B, E (366-m downwind) and F (538-m downwind). The eastward transect was generated using the normalized samples A and B, C (377-m downwind), D (657-m downwind) and N (786-m downwind). For the June sample period, the northward transect was generated by first averaging the sample concentrations collected at different downwind ranges, which included the AA samples (~205-m downwind), I, J, and BB samples (~300-m downwind) and the K, L and CC samples (~379-m downwind). The sample averaged concentrations at tailings, 205-m, 300-m and 379-m downwind were then normalized and used to generate the northward transect.
Table 2.
Measured total As and Pb concentrations measured in the dust collected by the inverted-disc samplers. Locations are shown in
Figure 1.
Table 2.
Measured total As and Pb concentrations measured in the dust collected by the inverted-disc samplers. Locations are shown in Figure 1.
Location | 4/21 to 5/22 Period Pb (ppm) | 6/11 to 7/09 Period Pb (ppm) | 6/11 to 7/09 Period As (ppm) |
---|
A | 332 | 903 | 1826 |
B | 981 | 1743 | 3856 |
C | 317 | 1037 | 1406 |
D | 454 | 775 | 1389 |
E | 130 | 317 | 132 |
F | 39.3 | 71.2 | 46.4 |
G | 506 | 1614 | 1311 |
H | 482 | 838 | 588 |
I | 217 | 435 | 586 |
J | 218 | 383 | 504 |
K | 234 | 342 | 465 |
L | 292 | 439 | 649 |
M | 41.9 | N/A | N/A |
N | 41.2 | 138 | 156 |
AA | N/A | 384 | 449 |
BB | N/A | 453 | 595 |
CC | N/A | 302 | 435 |
Figure 8.
Map of PM27 deposition predicted by the DFM for the forecast period 21 April to 22 May 2014. The color scale represents the natural log of the deposition flux. The tailings impoundment is outlined in black and the locations of the inverted-disc samplers are indicated. The grid points are spaced by 10.3-m and the domain has a total horizontal extent of 34.49142° to 34.51452° latitude and −112.26247° to −112.23939° longitude.
Figure 8.
Map of PM27 deposition predicted by the DFM for the forecast period 21 April to 22 May 2014. The color scale represents the natural log of the deposition flux. The tailings impoundment is outlined in black and the locations of the inverted-disc samplers are indicated. The grid points are spaced by 10.3-m and the domain has a total horizontal extent of 34.49142° to 34.51452° latitude and −112.26247° to −112.23939° longitude.
Figure 9.
Map of PM27 deposition predicted by the DFM for the forecast period 11 June to 9 July 2014. The color scale represents the natural log of deposition. The tailings impoundment is outlined in black and the location and sample label of the inverted-disc samplers are indicated. The grid points are spaced by 10.3-m and the domain has a total horizontal extent of 34.49142° to 34.51452° latitude and −112.26247° to −112.23939° longitude.
Figure 9.
Map of PM27 deposition predicted by the DFM for the forecast period 11 June to 9 July 2014. The color scale represents the natural log of deposition. The tailings impoundment is outlined in black and the location and sample label of the inverted-disc samplers are indicated. The grid points are spaced by 10.3-m and the domain has a total horizontal extent of 34.49142° to 34.51452° latitude and −112.26247° to −112.23939° longitude.
For the May sampling period we first averaged the sample concentrations of I and J (~300-m downwind) and K and L (~379-m downwind). The northward transect was then generated using the normalized samples A and B, H (205-m downwind), 300-m downwind average, 379-m downwind average, and M (1027-m downwind).
Results for the southward, eastward and northward cross sections for the May and June sample periods can be seen in
Figure 10. The southward cross sections of the model-predicted fractional reduction in deposition follow similar trends to the observed fractional reduction of As and Pb concentrations measured in the inverted-disc samplers. For the May sampling period, the forecast overestimated the relative amount of deposition located at the sample locations E and F. This was most likely caused by strong northeasterly winds associated with a synoptic scale weather system. This weather system produced precipitation in the region, which the WRF model failed to predict. The erroneous WRF weather forecast yielded an overestimation of windblown dust transport in the southwestward direction. For June, the DFM model accurately forecasts the relative reduction in As and Pb at the E and F sample locations.
The eastward transect shows that the model-predicted fractional reduction in deposition was similar to the observed fractional reduction of As and Pb concentrations for both the May and June sampling periods for samplers C and N. However, the DFM underestimated the fractional reduction sampler D for both monthly sampling periods (
Table 1). Sampler D is located just 10-m from the eastern edge of the lower tailings area and approximately 4-m lower in elevation. This proximity and lower elevation of sampler D to the lower tailings area increased the likelihood of eroded particles to gravitationally settle into this sampler.
Table 1 shows that sampler D had systematically large deposition fluxes measured during both sample periods. Size distributions of the collected dust could not be determined due to the lack of total material captured by the sampler. The increased likelihood of capturing tailing material most likely skewed the fractional As and Pb deposition measured by the sampler.
Figure 10.
Comparison of relative decreases in arsenic (blue dashed lines) and lead (blue solid lines) mass concentrations measured by the samplers versus the relative decreases of deposition flux forecast by the DFM (red lines) for the southward (A) eastward (B) and northward (C) cross sections for the 21 April to 22 May 2014 sample period and the southward (D) eastward (E) and northward (F) cross sections for the 11 June to 9 July 2014 sample periods.
Figure 10.
Comparison of relative decreases in arsenic (blue dashed lines) and lead (blue solid lines) mass concentrations measured by the samplers versus the relative decreases of deposition flux forecast by the DFM (red lines) for the southward (A) eastward (B) and northward (C) cross sections for the 21 April to 22 May 2014 sample period and the southward (D) eastward (E) and northward (F) cross sections for the 11 June to 9 July 2014 sample periods.
The northward transect shows a similar downwind pattern of reduction in the fractional As and Pb concentration (
Figure 10). The DFM overestimates the fractional reductions of Pb for the May sampling period and both As and Pb for the June sampling period. However, the DFM was significantly better estimating the relative reduction of As and Pb for the May sampling period when compared to June. For the May sampling period the DFM accurately predicted the fractional reduction in Pb concentrations for sampler M located approximately 1-km north of the tailings.
The highest concentrations of both As and Pb were measured by the inverted-disc samplers located on the tailings (A and B). In comparison, the DFM model predicts that the highest amount of tailing dust deposition should occur approximately 150 m north of sample point B. However the inverted-disc samplers show significant reduction in relative As and Pb between the tailings (A and B) and the points located about 205-m north (H and AA).
The DFM includes topographic slopes when calculating deposition rates to the surface. Using computational fluid dynamics modeling, Stovern
et al. [
10] showed that the slope of the ground significantly impacts deposition in this topographically complex region. The inverted-disc samplers were strategically placed in locations that were sloped for the northward transect. The samples located at 205-m, 300-m and 379-m were in down-sloping, up-sloping and down-sloping regions, respectively. The slope of the ground at 205-m, 300-m and 379-m is −5.7°, +15.1°, and −22.3° respectively with a slope length of 50 m. Thus, we would expect that the samples collected at 300 m should have systematically more deposition than the samplers at 379-m. However, we appear to see the opposite occurring in the May sampling period and relatively equal amounts of deposition in the June sampling period. One reason why the effects of topographic slope are not evident in the deposition patterns may be due to changes in surface roughness between the sampler locations at 300-m and 379-m. The samplers located on the up-sloping terrain at 300 m are surrounded by very sparse vegetation, usually less than a meter in height with large barren patches of soil. On the other hand, the samplers located in the down sloping region at 379-m are surrounded by significantly more vegetation including shrubs, bushes and trees that are typically 2–3 m in height. The model, however, uses a constant surface roughness of 0.1-m. Large surface roughness and obstructing objects capture airborne dust in two ways, it removes momentum from the mean flow slowing transport of airborne particulates allowing them to gravitationally settle, as well as directly capturing airborne dust through direct contact and impaction of the airborne dust. This severe change in surface roughness may explain the counterintuitive results from the samplers. Another possible reason might be the high natural variability in deposition may overwhelm the topographic effect.
3.3.3. Lead Isotope Analysis
Figure 11 and
Figure 12 show the lead isotopic ratios for the dust collected on the inverted-disc samplers for the May and June sampling periods, respectively. Dust samples A and B located on the tailings themselves have the same isotopic composition as the bulk tailings sample, implying the airborne lead captured in the samplers originated exclusively from the tailings, as expected.
Figure 11.
Lead isotopic ratios
208Pb/
206Pb and
207Pb/
206Pb for each inverted-disc sampler and a bulk sample of tailings material for the 21 April to 22 May 2014 sampling period. The letters represent the inverted-disc sample locations from
Figure 1. Tailings (surrounded by a black circle), represent “fingerprint” ratios of the source. The background sample (BG, surrounded by a red circle) corresponds to topsoil (0–3 mm) collected 5 km from the source and represents the natural Pb isotopic “fingerprint” of the region. Error bars represent standard deviations from triplicate samples. Additionally included is the growth curve (solid line) adapted from Chen
et al. [
23], that represents changes in lead isotopic composition with time due to radiogenic production from isotopes of uranium and thorium, which encompasses all possible Earth samples.
Figure 11.
Lead isotopic ratios
208Pb/
206Pb and
207Pb/
206Pb for each inverted-disc sampler and a bulk sample of tailings material for the 21 April to 22 May 2014 sampling period. The letters represent the inverted-disc sample locations from
Figure 1. Tailings (surrounded by a black circle), represent “fingerprint” ratios of the source. The background sample (BG, surrounded by a red circle) corresponds to topsoil (0–3 mm) collected 5 km from the source and represents the natural Pb isotopic “fingerprint” of the region. Error bars represent standard deviations from triplicate samples. Additionally included is the growth curve (solid line) adapted from Chen
et al. [
23], that represents changes in lead isotopic composition with time due to radiogenic production from isotopes of uranium and thorium, which encompasses all possible Earth samples.
Figure 12.
Lead isotopic ratios
208Pb/
206Pb and
207Pb/
206Pb for each inverted-disc sampler and a sample of tailings topsoil for the 11 June to 9 July 2014 sampling period. The letters represent the inverted-disc sample locations from
Figure 1. Tailings (surrounded by a black circle), represent “fingerprint” ratios of the source. The background sample (BG, surrounded by a red circle), corresponds to topsoil (0–3 mm) collected 5 km from the source and represents the natural Pb isotopic “fingerprint” of the region. Error bars represent standard deviations from triplicate samples. Additionally included is the growth curve (solid line) adapted from Chen
et al. [
23].
Figure 12.
Lead isotopic ratios
208Pb/
206Pb and
207Pb/
206Pb for each inverted-disc sampler and a sample of tailings topsoil for the 11 June to 9 July 2014 sampling period. The letters represent the inverted-disc sample locations from
Figure 1. Tailings (surrounded by a black circle), represent “fingerprint” ratios of the source. The background sample (BG, surrounded by a red circle), corresponds to topsoil (0–3 mm) collected 5 km from the source and represents the natural Pb isotopic “fingerprint” of the region. Error bars represent standard deviations from triplicate samples. Additionally included is the growth curve (solid line) adapted from Chen
et al. [
23].
Samples with lower isotopic ratios are the consequence of mixing between the tailings source and regional background. For the May sampling period, the samples that have the lowest isotope ratio are F and N. Sample F is the most southern sample located approximately 300-m from the southern edge of the tailings while N the eastern most sample is located approximately 150-m from the eastern-most edge of the lower tailings area. The small contribution of tailings lead measured in these samplers matches the monthly wind patterns that predominantly transported dust northward, away from the samplers. Samples M and E also have a significantly lower isotopic ratios than the tailing samples. It is interesting to note that sample E which is located only about 200 m from the southern edge of the tailings has the same fractional contribution of tailings lead as the sampler located 1 km north, as expected from the prevailing winds. Also, the source of lead captured by the inverted-disc sampler N, located along AZ highway 69 which separates the Iron King tailings and the town of Dewey-Humboldt, had a smaller tailings contribution than the sampler located 1 km north of the tailings.
For the June sampling period, the lead isotopic signatures were significantly closer to the tailings bulk sample when compared to the May sampling period. The samples with the lowest isotopic ratios included samples F, N and E. Sample F had the lowest lead contribution from the tailings, this matches the results from the May sampling period. However, more of the lead measured in sample F was sourced from the tailings compared to May. For the eastern most sampler, N and southern sampler E, the isotopic ratios were closer to the tailings signature as well, while still maintaining the lowest isotopic ratios of all the June samplers.
It is interesting to note that the June samplers had significantly higher lead concentrations and isotopic ratios when compared to May. This was caused by a precipitation event that occurred on April 27. This precipitation event significantly increased the tailings moisture content, minimizing wind erosion and reducing windblown lead deposition for the May sample period. In the June sample period the tailings had not received precipitation in over a month which significantly increasing the erosion potential, which resulted in more tailings sourced lead deposition causing the increase in lead concentrations and also shifting isotopic fingerprints closer to the tailings isotopic signature. This shows that local weather patterns including predominant wind directions and precipitation have a significant effect on the deposition of windblown dust from the Iron King tailings impoundment.
The lead isotope ratios can be used to calculate the contribution of deposited dust that originates in the tailings. Assuming only two different lead sources (tailings and background), the calculated fractional Pb tailings contribution was defined here as the ratio between the difference in the 207/206 ratio between the samples and the background, divided by the difference between the tailings and the background. Results are plotted as a function of predicted dust deposition fluxes in
Figure 13, for the two different sampling periods. Despite the scatter, a clear increasing relation is obtained between the proportion of dust originating in the tailings and the total deposition flux of tailings materials predicted by the model.
Lead isotopic ratios for the soil samples at different levels collected along the NE transect (
Figure 7) are shown in
Figure 14. Samples located 130 m from the tailings were collected in up-sloped terrain and their lead signatures are close to the tailings, indicating that the relatively high concentrations of lead (
Figure 7) are a consequence of dust transport from the tailings. At this distance, results from the DFM model also point to a high deposition of tailings dust (
Figure 10). It is interesting to point out that even at a depth of 100 mm, lead isotope analysis points to the tailings as main contributor of the metal in the soil. At longer distances from the tailing (1150 m), topsoil and 100-mm depth soil have significantly different signatures, with deep soil reflecting a higher contribution from the 5-km background. The sampling point located 13 m from the tailing has the same lead isotope ratios as the tailing topsoil, as expected, but isotopic ratios decrease monotonically with distance towards the background site located 5 km from the tailings.
Figure 13.
Calculated tailings contribution of deposited lead in inverted-disc samplers as a function of the model-predicted dust deposition flux for the two different sampling periods in 2014. Tailings contribution (1 for tailings, 0 for background) are calculated from the 207/206 isotopic ratios reported in
Figure 11 and
Figure 12.
Figure 13.
Calculated tailings contribution of deposited lead in inverted-disc samplers as a function of the model-predicted dust deposition flux for the two different sampling periods in 2014. Tailings contribution (1 for tailings, 0 for background) are calculated from the 207/206 isotopic ratios reported in
Figure 11 and
Figure 12.
Figure 14.
Lead isotopic ratios for soil samples at different distances from the mine tailings (indicated). Numbers in parentheses represent the depth of the sample in mm. Error bars represent standard deviations from triplicate samples. Additionally included is the growth curve (solid line) adapted from Chen
et al. [
23].
Figure 14.
Lead isotopic ratios for soil samples at different distances from the mine tailings (indicated). Numbers in parentheses represent the depth of the sample in mm. Error bars represent standard deviations from triplicate samples. Additionally included is the growth curve (solid line) adapted from Chen
et al. [
23].